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"Danish Demes"
Lineages and Results of Y-chromosome DNA Testing for a Regional Danish DNA Project
Haplogroup J2
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Y-DNA Haplogroups Represented in the Project
and Their Frequency (n tested at FTDNA + n tested elsewhere)
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F (1 + 0) G (2 + 0) I1 (17+ 1) I2 (5 + 0) J2 (1 + 0) R1a (3 + 1) R1b (16 + 0)

The J2 subclade of Haplogroup J (see entries at Wikipedia and ISOGG) arose in the northern Fertile Cresent, roughly 18,500 ±3500 years ago.  It then spread westwards around the Mediterranean and broadly eastwards throughout central Asia and south into India.  It is most common in Anatolia — about 25% of Turks are J2.   (See Figure 2, Map C, for distribution of J2).

We have one member of the Danish Demes proejct who is Haplogroup J2.  This haplogroup is so uncharacteristically Danish that it raises the question of whether his origin truly is Denmark.  He currently has no matches, but perhaps when he does we'll have an answer.

Haplogroup J Subclades as Defined by SNP Mutations
The chart below is a comparison of the Haplogroup J SNPs and subclade designations as given by ISOGG (the International Society of Genetic Genealogy) and as used by Family Tree DNA.  Our member is J2 by both classifications, at least until he undergoes deep SNP testing, which your project admin recommends.
Mutations New Clades
ISOGG FTDNA
M304 12f2a P209 S6 S34 S35 J J
__ M267 J1 J1
__ M62 J1a J1a
M365 J1b J1b
M390 J1c J1c
P56 J1d J1d
P58 J1e J1e
___ M367 M368 J1e1 J1e1
M369 J1e2 J1e2
M172 J2 J2
__ M410 J2a J2a
__ DYS413≤18 S57 J2a1  
__ M47 M322 J2a1a J2a1
M67 S51 J2a1b J2a2
__ M92 M260 J2a1b1 J2a2a
__ M327 J2a1b1a J2a2a1
M163 M166 J2a1b2 J2a2b
M68 J2a1c J2a3
M158 J2a1d J2a5
M319 J2a1e J2a8
M339 J2a1f J2a9
M419 J2a1g J2a11
DYS445≤7 J2a1h  
__ M137 J2a1h1 J2a4
M289 J2a1h2 J2a6
M318 J2a1h3 J2a7
P81 J2a1i J2a12
P279 J2a1j J2a13
M340 J2a2 J2a10
M12 M102 M221 M314 J2b J2b
__ M205 J2b1 J2b1
M241 J2b2 J2b2
__ M99 J2b2a J2b2a
M280 J2b2b J2b2b
M321 J2b2c J2b2c
P84 J2b2d J2b2d
DYS455≤9 J2b2e  

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Red labels indicate markers that typically mutate more frequently than those labeled in black. Marker 464 mutates most rapidly of all and sometimes has five to seven counts (a-g), not just four (a-d).
(Empty cells that are darkened indicate tests not ordered.)
Surname Kit # Ysearch
Code

SNP
Test
Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3
3
9
0
19
/
3
9
4
3
9
1
a
|
3
8
5
b
|
3
8
5
4
2
6
3
8
8
4
3
9
i
|
3
8
9
3
9
2
ii
|
3
8
9
4
5
8
a
|
4
5
9
b
|
4
5
9
4
5
5
4
5
4
4
4
7
4
3
7
4
4
8
4
4
9
a
|
4
6
4
b
|
4
6
4
c
|
4
6
4
d
|
4
6
4
4
6
0
H4
|
G
A
T
A
IIa
|
Y
C
A
IIb
|
Y
C
A
4
5
6
6
0
7
5
7
6
5
7
0
a
|
C
D
Y
b
|
C
D
Y
4
4
2
4
3
8
5
3
1
5
7
8
a
|
S1
3
9
5
b
|
S1
3
9
5
5
9
0
5
3
7
6
4
1
4
7
2
S1
4
0
6
5
1
1
4
2
5
a
|
4
1
3
b
|
4
1
3
5
5
7
5
9
4
4
3
6
4
9
0
5
3
4
4
5
0
4
4
4
4
8
1
5
2
0
4
4
6
6
1
7
5
6
8
4
8
7
5
7
2
6
4
0
4
9
2
5
6
5
J2 Modals 9EQTH   12 23 14 10 13 17 11 15 11 13 11 29 16 8 9 11 11 26 15 20 29 13 13 15 16 10 10 19 22 15 14 16 17 35 38 11 9                                                             Modals compiled by Al Aburto, Jr. (n=304).
                 
HANSEN 94599 UY744 M172+ 12 22 14 10 15 15 11 14 11 13 11 30 15 8 9 11 11 25 15 20 28 13 13 16 17 10 11 21 22 15 14 18 17 35 39 12 9                                                             Pvt4, Pvt3, Andrew2, Andrew1 — born in Iowa, parents born in DK
This individual has a unique haplotype, with no matches at any level in the FTDNA or Ysearch databases.  His closest match at Ysearch is with the J2 modal haplotype, yet his genetic distance from the modal is considerable.  Through four censuses, his earliest known ancestor consistently gives his parents' birthplaces as "Denmark"; however, this haplogroup is so atypically Danish, it raises the question as to whether this origin is correct.  It could also mean this individual has an NPE, a "non-paternal event" (i.e., hidden adoption or illicit paternity) in his lineage.  We'll have a better idea as more people are tested and he begins to have matches.  Perhaps some very adventurous J2's made it this far north.
   

What constitutes a match?
For 12 markers:  8 or less is a non-relative; 9-10 means only a small chance of a relationship; 11-12 means a possible relationship.
For 25 markers:  20 or less is a non-relative; 21-22 means only a small chance of a relationship; 23-25 means a possible relationship.
For 37 markers:  30 or less is a non-relative; 31-37, please see this Chart compiled by FTDNA.
For 67 markers:  55 or less is a non-relative; 58-67, please see this Chart compiled by FTDNA.
For any test:  0 matching markers, please contact NASA.

 
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