D7S820
D7S820 is a tetranucleotide short tandem repeat (STR) locus on chromosome 7 (7q21.11), one of the 20 CODIS core loci.
7
7q21.11
A[n]CTAT[1]CAATCTGT[1]CTAT[n]_-1T>-
Tetranucleotide
13
Explore internal sequence structure
See how the STRNaming name of the reference allele maps onto its sequence: repeat blocks, flanking regions and flanking variants.
See the reads at this locus
Open the built-in IGV viewer on the hg38 window of this marker with a 1000 Genomes sample.
GRCh38/hg38
chr7:84,160,226-84,160,277 (52 bp)
GRCh37/hg19
chr7:83,789,542-83,789,593 (52 bp)
Motif and sequences are shown on the forward (+) strand of GRCh38.
CE13_A[8]CTAT[1]CAATCTGT[1]CTAT[13]
[TATC]13
chr7:84,160,200-84,160,281 (82 bp)
- PowerSeq 46GY
- ForenSeq Signature Prep/Plus and MainstAY
- Precision ID GlobalFiler NGS STR Panel v2 (Does not cover the whole ISFG minimum range.)
- IDSeek OmniSTR Global
Kit range does not cover the whole ISFG minimum range of this locus (chr7:84,160,200-84,160,281), according to the kit ranges in the FSSG. Bases of the minimum range outside a kit's range are not sequenced by that kit; bases filled in from the reference should be identified as such.
Originally characterized on the reverse strand
- Africa
- Allele 10 (0.405, n = 505)
- Native American
- Allele 10 (0.299, n = 537)
- East Asia
- Allele 11 (0.348, n = 221)
- Central and South Asia
- Allele 10 (0.246, n = 193)
- Europe
- Allele 10 (0.256, n = 659)
- Middle East
- Allele 10 (0.325, n = 157)
- Oceania
- Allele 11 (0.278, n = 18)
| Allele | AFR | NAM | EAS | CSA | EUR | MES | OCE |
|---|---|---|---|---|---|---|---|
| 6 | 0.002 | 0 | 0 | 0 | 0 | 0 | 0 |
| 6.3 | 0 | 0.001 | 0 | 0 | 0 | 0 | 0 |
| 7 | 0.004 | 0.009 | 0 | 0.041 | 0.020 | 0.019 | 0 |
| 7.3 | 0.003 | 0 | 0 | 0 | 0 | 0 | 0 |
| 8 | 0.186 | 0.168 | 0.174 | 0.212 | 0.178 | 0.102 | 0.194 |
| 8.1 | 0.002 | 0 | 0 | 0 | 0 | 0 | 0 |
| 9 | 0.071 | 0.088 | 0.038 | 0.073 | 0.159 | 0.108 | 0.028 |
| 10 | 0.405 | 0.299 | 0.201 | 0.246 | 0.256 | 0.325 | 0.222 |
| 10.1 | 0.011 | 0 | 0 | 0 | 0 | 0 | 0 |
| 10.3 | 0.001 | 0.001 | 0 | 0 | 0 | 0 | 0 |
| 11 | 0.177 | 0.245 | 0.348 | 0.244 | 0.210 | 0.268 | 0.278 |
| 11.1 | 0.001 | 0 | 0 | 0 | 0 | 0 | 0 |
| 11.3 | 0.001 | 0 | 0 | 0 | 0 | 0 | 0 |
| 12 | 0.122 | 0.150 | 0.199 | 0.163 | 0.136 | 0.146 | 0.222 |
| 13 | 0.012 | 0.032 | 0.038 | 0.021 | 0.034 | 0.029 | 0.056 |
| 13.1 | 0 | 0.001 | 0 | 0 | 0 | 0 | 0 |
| 14 | 0.002 | 0.007 | 0 | 0 | 0.006 | 0.003 | 0 |
| 15 | 0 | 0.001 | 0 | 0 | 0 | 0 | 0 |
Allele frequencies by population group (pop.STR, CE). Alleles absent from every group are omitted.
STRbase reports 56 sequence variants across 19 allele designations.