D22S1045

CODIS Core

D22S1045 is a trinucleotide short tandem repeat (STR) locus on chromosome 22 (22q12.3), one of the 20 CODIS core loci.

Basic Information

22

22q12.3

ATT[n]ACT[1]ATT[2]

Trinucleotide

17

Explore internal sequence structure

See how the STRNaming name of the reference allele maps onto its sequence: repeat blocks, flanking regions and flanking variants.

Open STR Motif Explorer
Genomic Coordinates

GRCh38/hg38

chr22:37,140,287-37,140,337 (51 bp)

GRCh37/hg19

chr22:37,536,327-37,536,377 (51 bp)

Motif and sequences are shown on the forward (+) strand of GRCh38.

Sequence structure (FSSG)
ISFG minimum range, bracketing and kit coverage from the Forensic Sequence Structure Guide, FSSG v6.1 (STRidER; distributed as FSSG_v6-1_beta.xlsx).
ATT[n]ACT[1]ATT[2]

CE17_ATT[14]ACT[1]ATT[2]

[ATT]14 ACT [ATT]2

chr22:37,140,283-37,140,341 (59 bp)

  • PowerSeq 46GY
  • ForenSeq Signature Prep/Plus and MainstAY
  • Precision ID GlobalFiler NGS STR Panel v2
  • IDSeek OmniSTR Global
Allele frequencies at a glance
Most common allele per population group, with its frequency and the sample size, in the capillary electrophoresis data of pop.STR / SP-SMART.
Africa
Allele 17 (0.275, n = 102)
Native American
Allele 15 (0.349, n = 546)
East Asia
Allele 11 (0.268, n = 226)
Central and South Asia
Allele 15 (0.380, n = 200)
Europe
Allele 15 (0.334, n = 1,820)
Middle East
Allele 15 (0.411, n = 151)
Oceania
Allele 15 (0.479, n = 24)
Allele frequencies by population group (pop.STR, CE). Alleles absent from every group are omitted.
AlleleAFRNAMEASCSAEURMESOCE
800.001000.00100
90000.0050.00100
100.0880.0380.0020.0050.0120.0100
110.1570.1030.2680.2330.1290.1290.021
120.0290.0300.0020.0030.0200.0430
130.0200.0030.0040.0030.0050.0030.063
140.0640.0630.0270.0830.0480.0460
150.1860.3490.2520.3800.3340.4110.479
160.1670.2660.2460.2230.3100.2910.313
170.2750.1340.1790.0600.1290.0500.104
180.0100.0120.0150.0070.0090.0170.021
190.0050.0010.00400.00200

Allele frequencies by population group (pop.STR, CE). Alleles absent from every group are omitted.

Variant Alleles

STRbase reports 27 sequence variants across 13 allele designations.

8
9
10
11
12
13
14
15
15.1
16
17
18
19