Results for: Albertus
(Bert) - S300059All
from Relative Genetics Laboratory
Locus 1 2
3 4 5
6 7 8 9
10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26
Value
11 15 12 13 29 25 11 13 13
14 12 15 12 12 26 11 11 11 12 11 09 14 24 12 19 23
Locus 27 28
29 30 31
32 33 34
35 36 37
38 39 40 41 42
43
Value 14
17 12 12 13
19 30 30 15
19 09 10
25 15 15 16
17
Locus (Marker)Key (1-26)
1) DYS385a 5) DYS389II
9) DYS393 13) DYS438 17) DYS455 21) GGAAT1B07
2) DYS385b
6) DYS390
10) DYS19 14) DYS439 18) DYS460 22) GATAA10
3) DYS388 7) DYS391 11) DYS426 15)
DYS447 19) DYS461 23) DYS635
4) DYS389I 8) DYS392
12) DYS437
16) DYS454 20) DYS462
24) GATAH4.1
25) YCAIIa 26) YCAIIb
Locus (Marker) Key
(27-43, added in Sep 2004)
27) DYS441 31) DYS446 35) DYS456 39) DYS463 43) DYS464d
28) DYS442 32) DYS448 36) DYS458 40) DYS464a
29) DYS444 33) DYS449 37) DYS459a 41)
DYS464b
30) DYS445 34) DYS452 38) DYS459b 42)
DYS464c
Notes to the Marker Key
1) DYS385a – the value, originally B, was
converted to 11.
2) DYS385b – the value, originally F, was
converted to 15.
4) DYS389I - the original value 12, was
increased by 1, to 13
10) DYS19 – was formerly known as DYS394.
15) DYS447 – not one of the original 26, was added
later.
19) DYS461 – in June 2004 this value was increased by 1,
to 12.
23) DYS635 – this marker was known until July 2004 as
YGATAC4.
24) YGATAH4 –
originally 27, this value was decreased by 15, to 12, and since June 2004 has
been known as TAGA H4.
25) YCAIIa – originally
D, was converted to 19.
26) YCAIIb – originally
H, was converted to 23.
Postscriptum: as of dec 2007 several scores have been
changed by the laboratories, as follows:
27) DYS441 -
formerly 13, has been increased by one to 14.
28) DYS442 -
formerly 12, has been increased by five to 17.
34) DYS452 -
formerly 11, has been increased to 30.
39) DYS463 -
formerly 23, has been increased to 25.
12) GATA-A10 –
formerly 12, has been increased to 14.
24) GATA-H4.1 –
until 2004 this marker was known as YGATAH4; between 2004 and Dec 2007 as TAGA
H4; its value – at first 27, was later reduced to 12, and then increased again
to 22; in 2009 was this marker renamed GATAH4, and the value was reduced by 10,
thus, in my case, to 12.
On 24 Feb 2002 at my home in
Amsterdam I swabbed the inside of my mouth with a cotton stick provided by the
Laboratory of Relative Genetics. I sent the sample in to them on the following
day. This report presents my Paternal Ancestry Signature as revealed by
analysing 26 (later, 43) different locations on my Y-chromosome. The
fascinating aspect of the Paternal Ancestry Signature is that it does not
uniquely identify me as a single individual, but uniquely identifies my
paternal line back through history that extends beyond written records, as the
Y-chromosome is passed down intact from father to son through many generations.
The Paternal Ancestry Signature is made up of 26 (later, 43) different data
points (called loci or markers) that are analysed
for the number of repeats at the location. These repeats are known as STR’s
(Short Tandem Repeats). (Some markers have multiple alleles. Thus, 385a and b
are actually one marker with two alleles, as are 459a & b; 464a, b, c &
d; and YCAII a & b.)
In July 2004 I did another
DNA test at my home, this time with DNA Heritage in England. My test values for
the 43 markers of DNA Heritage happily coincide with my test values of the
corresponding markers of Relative Genetics (see hereunder):
Marker |
DYS19 |
DYS385 |
DYS388 |
DYS389I |
DYS389II |
DYS390 |
DYS391 |
DYS392 |
DYS393 |
DYS426 |
Value |
14 |
11-15 |
12 |
13 |
29 |
25 |
11 |
13 |
13 |
12 |
Marker |
DYS437 |
DYS438 |
DYS439 |
DYS441 |
DYS442 |
DYS444 |
DYS445 |
DYS446 |
DYS447 |
DYS448 |
Value |
15 |
12 |
12 |
13 |
12 |
12 |
12 |
13 |
26 |
19 |
Marker |
DYS449 |
DYS452 |
DYS454 |
DYS455 |
DYS456 |
DYS458 |
DYS459 |
DYS460 |
DYS461 |
DYS462 |
||||||
Value |
30 |
30 |
11 |
11 |
15 |
19 |
9-10 |
11 |
12 |
11 |
||||||
Marker |
DYS463 |
DYS464 |
DYS635 |
Y-GATA-A10 |
Y-GATA-H4 |
Y-GGAAT-1B07 |
YCAII |
|||||||||
Value |
25 |
15-15-16-17 |
24 |
12 |
11 |
9 |
19-23 |
|||||||||
Relative Genetics genetic genealogy company was taken over by AncestryDNA
in 2008. Some projects hosted at Relative Genetics were transferred to DNA Heritage.
DNA Heritage in turn was acquired by Family Tree DNA
in April 2011. On 1 July 2011 my Y-Chromosome test results
were transferred, and the number of markers reduced from 43 to 25. FTDNA also
determined my Haplotype to be R1b1a2 (in 2014
renamed
R-M269), and my deep genetic ancestry to be 100 percent European (circa 87
percent ‘western european’, circa 13 percent ‘other european’). On 12
Dec 2013 I finally upgraded from Y-DNA 25 to Y-DNA 37 markers. The results for
all 37 markers, ready on 23 Jan 2014, can be seen hereunder:
Marker
|
DYS393
|
DYS390
|
DYS19** |
DYS391
|
DYS385
|
DYS426
|
DYS388
|
DYS439
|
DYS389I
|
DYS392
|
DYS389II*** |
Value |
13 |
25 |
14 |
11 |
11-15 |
12 |
12 |
12 |
13 |
13 |
29 |
Marker
|
DYS458
|
DYS459
|
DYS455
|
DYS454
|
DYS447
|
DYS437
|
DYS448
|
DYS449
|
DYS464
|
Value |
19 |
9-10 |
11 |
11 |
26 |
15 |
19 |
30about 20 000 |
15-15-16-17 |
Marker
|
DYS460
|
Y-GATA-H4
|
YCAII
|
DYS456
|
DYS607
|
DYS576
|
DYS570
|
CDY |
DYS442
|
DYS438
|
Value |
11 |
11 |
19-23 |
15 |
15 |
17 |
18 |
37-37 |
12 |
12 |
Marker |
DYS393 |
DYS390 |
DYS19** |
DYS391 |
DYS385 |
DYS426 |
DYS388 |
DYS439 |
DYS389I |
DYS392 |
DYS389II*** |
Value |
13 |
25 |
14 |
11 |
11-15 |
12 |
12 |
12 |
13 |
13 |
29 |
Marker |
DYS458 |
DYS459 |
DYS455 |
DYS454 |
DYS447 |
DYS437 |
DYS448 |
DYS449 |
DYS464 |
Value |
19 |
9-10 |
11 |
11 |
26 |
15 |
19 |
30 |
15-15-16-17 |
Marker |
DYS460 |
Y-GATA-H4 |
YCAII |
DYS456 |
DYS607 |
DYS576 |
DYS570 |
CDY |
DYS442 |
DYS438 |
Value |
11 |
11 |
19-23 |
15 |
15 |
17 |
18 |
37-37 |
12 |
12 |
Marker |
DYS531 |
DYS578 |
DYF395S1 |
DYS590 |
DYS537 |
DYS641 |
DYS472 |
DYF406S1 |
DYS511 |
Value |
11 |
9 |
15-16 |
9 |
10 |
10 |
8 |
11 |
10 |
Marker |
DYS425 |
DYS413 |
DYS557 |
DYS594 |
DYS436 |
DYS490 |
DYS534 |
DYS450 |
DYS444 |
DYS481 |
DYS520 |
DYS446 |
Value |
12 |
23-23 |
16 |
10 |
12 |
12 |
15 |
8 |
12 |
22 |
20 |
13 |
Marker |
DYS617 |
DYS568 |
DYS487 |
DYS572 |
DYS640 |
DYS492 |
DYS565 |
Value |
12 |
11 |
13 |
11 |
11 |
12 |
12 |
In February 2016 I ordered the AncestryDNA
saliva test kit for autosomal DNA testing. AncestryDNA has determined that I am over 99 percent European, to wit:
Western Continental Europe – 67%, Ireland – 14%, Scandinavia – 12% (updated in 2018 to 100%
European, to wit: England
& Northestern Europe – 93%, Norway – 3%, Germanic Europe – 2%, Sweden – 2%). As of June 2016,
at AncestryDNA I already had ninety genetically and
genealogically confirmed maternal cousin matches of various degrees from First
Cousin to Ninth Cousin. I also had two paternal 2nd Cousins 1R,
several paternal 3rd Cousin, and several paternal 4th
Cousin DNA matches. Through DNA matching and genetic genealogy I was able to
determine and confirm the identity of my father’s parents, his four
grandparents, his eight great-grandparents, and six of his
great-great-grandparents; I was also able to narrow down the identity of my
father to one of two brothers – H. & D. -
both sons of Frank Casimir Jung. A 3rd
Cousin DNA match at AncestryDNA graciously put me
into contact with the grandson of H., the elder son of Frank Jung. Not only did
he share with me photographs and information on my paternal family of origin,
but he also offered to the AncestryDNA test. On
Easter Sunday (17 April) 2017 his DNA test results became known: he and I share
312 centiMorgans
across 19 DNA segments. He proved to be my closest paternal match yet, my First Cousin Once
Removed, thus confirming that his granduncle D. Jung, the younger of the two
sons of Frank Jung, is my father. DNA matching combined with family tree
analysis is a powerful tool indeed! And today I feel like very blessed indeed
to have been so helped by it. Moreover, in 2017, by using the same combined
method of DNA matching and family tree analysis, I was able to find out who the
fathers were of four of my maternal brothers.
In the summer
of 2017, J. B. Young, a paternal Third Cousin of mine, a direct male descendant of Casimir Jung
in the surname line, as am I, whose relationship to me had already been proven
by Autosomal DNA testing at AncestryDNA,
agreed to do the FTDNA Y-Chromosome Test. On 28 September 2017 the results
became known: his 37 markers matched my 37 markers perfectly, at a distance of
0, thereby confirming our direct paternal surname
line. Thus, the Y-Chromosome Test affirms that both of us should bear the same
surname ‘’Jung’’: he, in fact, does bear the ‘’Jung’’ surname in its anglicised
form: ‘’Young’’; myself, on the other hand, though I bear a different legal
surname through adoption, use with pride, whenever I can, the surname that is
mine by birthright, and mine by scientific proof: ‘’Jung’’.
Using the Results
of the Y Chromosome Matches
The raw numbers begin to take on genealogical significance when the
results are compared with other people and population studies. My full Paternal
Ancestry Signature is like a family fingerprint that identifies my paternal
male relatives, i.e., who share a common forefather with me on the direct
paternal line (my father’s father’s father’s father, for example). All other ancestors play no
part whatsoever in passing down the Y-chromosome, thus these test results say
absolutely nothing about them. Hopefully these test results will be compared to
the test results of many others. A perfect match of my Y-chromosome’s markers
with the markers of another’s Y-chromosome will prove that we are related to
each other in direct descent from a common male ancestor on our father’s side within
eight generations counting from my generation backwards in time, and that
we should share the same surname (keeping in mind, however, that non-paternal
events would influence the surname). One value off on one marker (a mutation)
would still indicate blood relationship and descent from a common forefather,
but more likely at eight or more generations back in time. (The
number of generations is not definite, but based on probabilities, as it is
still not known precisely how often or seldom in time a mutation takes place).
In Europe there are three main Haplogroups: HG1, HG2,
HG3. A haplogroup is a collection of closely related
haploid cell genotypes (haplotypes). As science
progresses, so does our knowledge of these haplogroups:
thus their names and descriptions are ever-changing.
.
North-Western Europe - geographic place of origins of
my Y-Chromosome, Autosomal DNA & mtDNA
Percentage of Haplogroup
R-M269‘s presence in Europe by region
The newest information on haplotype
R1b1a2 (R-M269) (Jan 2014 update)
Prior to 2002,
today's Haplogroup R1b had a number of names in differing
nomenclature systems, such as Hg1 and Eu18. From 2003 to 2005
what is now R1b1a2
was designated R1b3. From 2005 to 2008 it was R1b1c. From 2008 to 2011 it was
R1b1b2. R1b1a2 (2011 name) is defined by the presence of SNP marker M269.
European R1b is dominated by R-M269.
The frequency is about 50% in Germany and Holland, 60% in France, 70% in
Scotland and Spain. In south-eastern England the frequency of this clade is about 70%; in parts of the rest of north and
western England, Spain, Portugal, Wales and Ireland, it is as high as 90%; and
in parts of north-western Ireland it reaches 98%. This haplogroup’s
presence is highest in Western Europe and gradually decreases eastward.
[Source: http://en.wikipedia.org/wiki/Haplogroup_R1b_(Y-DNA)
]
For further information on the subject of
genetic genealogy:
http://dnaadoption.com.gerbera.arvixe.com/Home.aspx
http://www.isogg.org/wiki/AncestryDNA
http://www.isogg.org/wiki/Y-DNA_STR_testing_chart
http://www.isogg.org/wiki/Autosomal_DNA_testing_comparison_chart
http://www.clanlindsay.com/genetic_dna_glossary.htm
http://www.pnas.org/cgi/reprint/98/9/5078.pdf
For information on U-152:
http://www.eupedia.com/forum/threads/25962-R1b-U152-S28-more-Gaulish-or-Roman
http://www.davidkfaux.org/R1b1c10_Resources.pdf
And for possible DNA matches see this
on-line Y-chromosome database: