esv2421437
- Organism: Homo sapiens
- Study:estd195 (Altshuler et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:23
- Validation:Not tested
- Clinical Assertions: No
- Region Size:8,871
- Publication(s):International HapMap 3 Consortium et al. 2010
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 171 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 35 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 177 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 38 SVs from 15 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
esv2421437 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
esv2421437 | Remapped | Perfect | GRCh38.p12 | PATCHES | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
esv2421437 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
esv2421437 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
---|---|---|---|---|---|---|
essv5005621 | deletion | NA19403 | SNP array | SNP genotyping analysis | 1 | 145 |
essv5017139 | deletion | NA20358 | SNP array | SNP genotyping analysis | 1 | 150 |
essv5021859 | deletion | NA19176 | SNP array | SNP genotyping analysis | 1 | 162 |
essv5043492 | deletion | NA20333 | SNP array | SNP genotyping analysis | 1 | 146 |
essv5045329 | deletion | NA19471 | SNP array | SNP genotyping analysis | 1 | 138 |
essv5053282 | deletion | NA20356 | SNP array | SNP genotyping analysis | 1 | 150 |
essv5054433 | deletion | NA20288 | SNP array | SNP genotyping analysis | 1 | 144 |
essv5055585 | deletion | NA19161 | SNP array | SNP genotyping analysis | 1 | 155 |
essv5065423 | deletion | NA19143 | SNP array | SNP genotyping analysis | 1 | 143 |
essv5065649 | deletion | NA19121 | SNP array | SNP genotyping analysis | 1 | 133 |
essv5085125 | deletion | NA19213 | SNP array | SNP genotyping analysis | 1 | 137 |
essv5091852 | deletion | NA19472 | SNP array | SNP genotyping analysis | 1 | 137 |
essv5093709 | deletion | NA19718 | SNP array | SNP genotyping analysis | 1 | 115 |
essv5097481 | deletion | NA21524 | SNP array | SNP genotyping analysis | 1 | 149 |
essv5099042 | deletion | NA19095 | SNP array | SNP genotyping analysis | 0 | 158 |
essv5099353 | deletion | NA20332 | SNP array | SNP genotyping analysis | 1 | 143 |
essv5108870 | deletion | NA19327 | SNP array | SNP genotyping analysis | 1 | 151 |
essv5113616 | deletion | NA19204 | SNP array | SNP genotyping analysis | 1 | 146 |
essv5131715 | deletion | NA19123 | SNP array | SNP genotyping analysis | 1 | 143 |
essv5141876 | deletion | NA19160 | SNP array | SNP genotyping analysis | 1 | 147 |
essv5142834 | deletion | NA21295 | SNP array | SNP genotyping analysis | 1 | 139 |
essv5146125 | deletion | NA19468 | SNP array | SNP genotyping analysis | 1 | 130 |
essv5150439 | deletion | NA19097 | SNP array | SNP genotyping analysis | 1 | 146 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv5005621 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5017139 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5021859 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5043492 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5045329 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5053282 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5054433 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5055585 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5065423 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5065649 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5085125 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5091852 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5093709 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5097481 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5099042 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5099353 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5108870 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5113616 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5131715 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5141876 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5142834 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5146125 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5150439 | Remapped | Perfect | NW_011332687.1:g.( ?_211144)_(220014_ ?)del | GRCh38.p12 | Second Pass | NW_011332687.1 | Chr1|NW_01 1332687.1 | 211,144 | 220,014 |
essv5005621 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5017139 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5021859 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5043492 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5045329 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5053282 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5054433 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5055585 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5065423 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5065649 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5085125 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5091852 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5093709 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5097481 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5099042 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5099353 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5108870 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5113616 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5131715 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5141876 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5142834 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5146125 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5150439 | Remapped | Perfect | NC_000001.11:g.(?_ 210431402)_(210440 272_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 210,431,402 | 210,440,272 |
essv5005621 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5017139 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5021859 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5043492 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5045329 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5053282 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5054433 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5055585 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5065423 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5065649 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5085125 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5091852 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5093709 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5097481 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5099042 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5099353 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5108870 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5113616 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5131715 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5141876 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5142834 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5146125 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5150439 | Remapped | Perfect | NC_000001.10:g.(?_ 210604746)_(210613 616_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 210,604,746 | 210,613,616 |
essv5005621 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5017139 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5021859 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5043492 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5045329 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5053282 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5054433 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5055585 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5065423 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5065649 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5085125 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5091852 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5093709 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5097481 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5099042 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5099353 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5108870 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5113616 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5131715 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5141876 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5142834 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5146125 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 | ||
essv5150439 | Submitted genomic | NC_000001.9:g.(?_2 08671369)_(2086802 39_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 208,671,369 | 208,680,239 |