esv2761322
- Organism: Homo sapiens
- Study:estd203 (Vogler et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:37
- Validation:Not tested
- Clinical Assertions: No
- Region Size:4,366
- Publication(s):Vogler 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: 503 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 503 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 257 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2761322 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 23,055,011 | 23,059,376 |
| esv2761322 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 23,629,150 | 23,633,515 |
| esv2761322 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 22,527,150 | 22,531,515 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv6997747 | copy number loss | SW_1004 | SNP array | SNP genotyping analysis | 31 |
| essv6997748 | copy number loss | SW_0021 | SNP array | SNP genotyping analysis | 39 |
| essv6997749 | copy number loss | SW_0045 | SNP array | SNP genotyping analysis | 39 |
| essv6997750 | copy number loss | SW_0062 | SNP array | SNP genotyping analysis | 31 |
| essv6997751 | copy number loss | SW_0063 | SNP array | SNP genotyping analysis | 48 |
| essv6997752 | copy number loss | SW_0103 | SNP array | SNP genotyping analysis | 37 |
| essv6997753 | copy number loss | SW_0121 | SNP array | SNP genotyping analysis | 31 |
| essv6997754 | copy number loss | SW_0189 | SNP array | SNP genotyping analysis | 53 |
| essv6997755 | copy number loss | SW_0203 | SNP array | SNP genotyping analysis | 49 |
| essv6997757 | copy number loss | SW_0286 | SNP array | SNP genotyping analysis | 29 |
| essv6997758 | copy number loss | SW_0351 | SNP array | SNP genotyping analysis | 27 |
| essv6997759 | copy number loss | SW_0554 | SNP array | SNP genotyping analysis | 29 |
| essv6997760 | copy number loss | SW_0590 | SNP array | SNP genotyping analysis | 55 |
| essv6997761 | copy number loss | SW_0619 | SNP array | SNP genotyping analysis | 31 |
| essv6997762 | copy number loss | SW_0623 | SNP array | SNP genotyping analysis | 40 |
| essv6997763 | copy number loss | SW_0663 | SNP array | SNP genotyping analysis | 52 |
| essv6997764 | copy number loss | SW_0674 | SNP array | SNP genotyping analysis | 38 |
| essv6997765 | copy number loss | SW_0773 | SNP array | SNP genotyping analysis | 37 |
| essv6997766 | copy number loss | SW_0814 | SNP array | SNP genotyping analysis | 36 |
| essv6997768 | copy number loss | SW_0832 | SNP array | SNP genotyping analysis | 41 |
| essv6997769 | copy number loss | SW_0889 | SNP array | SNP genotyping analysis | 27 |
| essv6997770 | copy number loss | SW_1042 | SNP array | SNP genotyping analysis | 33 |
| essv6997771 | copy number loss | SW_1051 | SNP array | SNP genotyping analysis | 61 |
| essv6997772 | copy number loss | SW_1059 | SNP array | SNP genotyping analysis | 23 |
| essv6997773 | copy number loss | SW_1080 | SNP array | SNP genotyping analysis | 35 |
| essv6997774 | copy number loss | SW_1086 | SNP array | SNP genotyping analysis | 35 |
| essv6997775 | copy number loss | SW_1120 | SNP array | SNP genotyping analysis | 26 |
| essv6997776 | copy number loss | SW_1170 | SNP array | SNP genotyping analysis | 42 |
| essv6997777 | copy number loss | SW_1180 | SNP array | SNP genotyping analysis | 43 |
| essv6997779 | copy number loss | SW_1198 | SNP array | SNP genotyping analysis | 39 |
| essv6997780 | copy number loss | SW_1236 | SNP array | SNP genotyping analysis | 23 |
| essv6997781 | copy number loss | SW_1254 | SNP array | SNP genotyping analysis | 27 |
| essv6997782 | copy number loss | SW_1278 | SNP array | SNP genotyping analysis | 28 |
| essv6997783 | copy number loss | SW_1290 | SNP array | SNP genotyping analysis | 54 |
| essv6997784 | copy number loss | SW_1381 | SNP array | SNP genotyping analysis | 32 |
| essv6997785 | copy number loss | SW_1387 | SNP array | SNP genotyping analysis | 24 |
| essv6997786 | copy number loss | SW_1452 | SNP array | SNP genotyping analysis | 40 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv6997747 | Remapped | Perfect | NC_000013.11:g.(?_ 23055011)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,055,011 | 23,059,376 |
| essv6997748 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997749 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997750 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997751 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997752 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997753 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997754 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997755 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997757 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997758 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997759 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997760 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997761 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997762 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997763 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997764 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997765 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997766 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997768 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997769 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997770 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997771 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997772 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997773 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997774 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997775 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997776 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997777 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997779 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997780 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997781 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997782 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997783 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997784 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997785 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997786 | Remapped | Perfect | NC_000013.11:g.(?_ 23058539)_(2305937 6_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 23,058,539 | 23,059,376 |
| essv6997747 | Remapped | Perfect | NC_000013.10:g.(?_ 23629150)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,629,150 | 23,633,515 |
| essv6997748 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997749 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997750 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997751 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997752 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997753 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997754 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997755 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997757 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997758 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997759 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997760 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997761 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997762 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997763 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997764 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997765 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997766 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997768 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997769 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997770 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997771 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997772 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997773 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997774 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997775 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997776 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997777 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997779 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997780 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997781 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997782 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997783 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997784 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997785 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997786 | Remapped | Perfect | NC_000013.10:g.(?_ 23632678)_(2363351 5_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 23,632,678 | 23,633,515 |
| essv6997747 | Submitted genomic | NC_000013.9:g.(?_2 2527150)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,527,150 | 22,531,515 | ||
| essv6997748 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997749 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997750 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997751 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997752 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997753 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997754 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997755 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997757 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997758 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997759 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997760 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997761 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997762 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997763 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997764 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997765 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997766 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997768 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997769 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997770 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997771 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997772 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997773 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 | ||
| essv6997774 | Submitted genomic | NC_000013.9:g.(?_2 2530678)_(22531515 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 22,530,678 | 22,531,515 |