esv2763649
- Organism: Homo sapiens
- Study:estd203 (Vogler et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:32
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,118,100
- 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: 3242 SVs from 102 studies. See in: genome view
Overlapping variant regions from other studies: 3253 SVs from 102 studies. See in: genome view
Overlapping variant regions from other studies: 828 SVs from 32 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2763649 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 86,893,372 | 88,011,471 |
| esv2763649 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 87,120,495 | 88,310,990 |
| esv2763649 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 86,974,006 | 88,092,105 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv7015155 | copy number gain | SW_0760 | SNP array | SNP genotyping analysis | 44 |
| essv7015166 | copy number gain | SW_1472 | SNP array | SNP genotyping analysis | 39 |
| essv7015177 | copy number gain | SW_1121 | SNP array | SNP genotyping analysis | 19 |
| essv7015190 | copy number gain | SW_1305 | SNP array | SNP genotyping analysis | 30 |
| essv7015201 | copy number gain | SW_1045 | SNP array | SNP genotyping analysis | 49 |
| essv7015212 | copy number gain | SW_1287 | SNP array | SNP genotyping analysis | 27 |
| essv7015223 | copy number gain | SW_1090 | SNP array | SNP genotyping analysis | 23 |
| essv7015234 | copy number gain | SW_0659 | SNP array | SNP genotyping analysis | 35 |
| essv7015245 | copy number gain | SW_1104 | SNP array | SNP genotyping analysis | 29 |
| essv7015256 | copy number gain | SW_1156 | SNP array | SNP genotyping analysis | 48 |
| essv7015267 | copy number gain | SW_0169 | SNP array | SNP genotyping analysis | 40 |
| essv7015278 | copy number gain | SW_0813 | SNP array | SNP genotyping analysis | 46 |
| essv7015289 | copy number loss | SW_1083 | SNP array | SNP genotyping analysis | 29 |
| essv7015301 | copy number gain | SW_1235 | SNP array | SNP genotyping analysis | 26 |
| essv7015312 | copy number gain | SW_1345 | SNP array | SNP genotyping analysis | 41 |
| essv7015323 | copy number gain | SW_0717 | SNP array | SNP genotyping analysis | 24 |
| essv7015334 | copy number gain | SW_0063 | SNP array | SNP genotyping analysis | 48 |
| essv7015345 | copy number gain | SW_1054 | SNP array | SNP genotyping analysis | 30 |
| essv7015356 | copy number gain | SW_1147 | SNP array | SNP genotyping analysis | 41 |
| essv7015367 | copy number gain | SW_0665 | SNP array | SNP genotyping analysis | 28 |
| essv7015378 | copy number gain | SW_1348 | SNP array | SNP genotyping analysis | 26 |
| essv7015389 | copy number gain | SW_1551 | SNP array | SNP genotyping analysis | 22 |
| essv7015400 | copy number gain | SW_0003 | SNP array | SNP genotyping analysis | 37 |
| essv7015412 | copy number gain | SW_1381 | SNP array | SNP genotyping analysis | 32 |
| essv7015423 | copy number gain | SW_0841 | SNP array | SNP genotyping analysis | 37 |
| essv7015434 | copy number loss | SW_1412 | SNP array | SNP genotyping analysis | 30 |
| essv7015445 | copy number gain | SW_0836 | SNP array | SNP genotyping analysis | 50 |
| essv7015456 | copy number gain | SW_1106 | SNP array | SNP genotyping analysis | 34 |
| essv7015467 | copy number loss | SW_1021 | SNP array | SNP genotyping analysis | 40 |
| essv7015478 | copy number loss | SW_0759 | SNP array | SNP genotyping analysis | 44 |
| essv7015489 | copy number loss | SW_0185 | SNP array | SNP genotyping analysis | 43 |
| essv7015500 | copy number loss | SW_0340 | SNP array | SNP genotyping analysis | 19 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv7015155 | Remapped | Perfect | NC_000002.12:g.(?_ 86893372)_(8772514 8_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 86,893,372 | 87,725,148 |
| essv7015166 | Remapped | Perfect | NC_000002.12:g.(?_ 87023373)_(8769685 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,023,373 | 87,696,853 |
| essv7015177 | Remapped | Perfect | NC_000002.12:g.(?_ 87051761)_(8769685 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,051,761 | 87,696,853 |
| essv7015190 | Remapped | Perfect | NC_000002.12:g.(?_ 87094919)_(8775281 1_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,094,919 | 87,752,811 |
| essv7015201 | Remapped | Perfect | NC_000002.12:g.(?_ 87110846)_(8772514 8_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,110,846 | 87,725,148 |
| essv7015212 | Remapped | Perfect | NC_000002.12:g.(?_ 87110846)_(8775281 1_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,110,846 | 87,752,811 |
| essv7015223 | Remapped | Perfect | NC_000002.12:g.(?_ 87117615)_(8769685 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,117,615 | 87,696,853 |
| essv7015234 | Remapped | Perfect | NC_000002.12:g.(?_ 87134049)_(8767494 4_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,134,049 | 87,674,944 |
| essv7015245 | Remapped | Perfect | NC_000002.12:g.(?_ 87134049)_(8767494 4_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,134,049 | 87,674,944 |
| essv7015256 | Remapped | Perfect | NC_000002.12:g.(?_ 87134049)_(8767494 4_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,134,049 | 87,674,944 |
| essv7015267 | Remapped | Perfect | NC_000002.12:g.(?_ 87134049)_(8769685 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,134,049 | 87,696,853 |
| essv7015278 | Remapped | Perfect | NC_000002.12:g.(?_ 87134049)_(8769685 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,134,049 | 87,696,853 |
| essv7015289 | Remapped | Perfect | NC_000002.12:g.(?_ 87134049)_(8769685 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,134,049 | 87,696,853 |
| essv7015301 | Remapped | Perfect | NC_000002.12:g.(?_ 87134049)_(8775281 1_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,134,049 | 87,752,811 |
| essv7015312 | Remapped | Perfect | NC_000002.12:g.(?_ 87134049)_(8775281 1_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,134,049 | 87,752,811 |
| essv7015323 | Remapped | Perfect | NC_000002.12:g.(?_ 87146770)_(8767494 4_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,146,770 | 87,674,944 |
| essv7015334 | Remapped | Perfect | NC_000002.12:g.(?_ 87146770)_(8769685 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,146,770 | 87,696,853 |
| essv7015345 | Remapped | Perfect | NC_000002.12:g.(?_ 87146770)_(8769685 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,146,770 | 87,696,853 |
| essv7015356 | Remapped | Perfect | NC_000002.12:g.(?_ 87146770)_(8769685 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,146,770 | 87,696,853 |
| essv7015367 | Remapped | Perfect | NC_000002.12:g.(?_ 87146770)_(8775281 1_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,146,770 | 87,752,811 |
| essv7015378 | Remapped | Perfect | NC_000002.12:g.(?_ 87244720)_(8772514 8_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,244,720 | 87,725,148 |
| essv7015389 | Remapped | Perfect | NC_000002.12:g.(?_ 87248317)_(8769685 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,248,317 | 87,696,853 |
| essv7015400 | Remapped | Perfect | NC_000002.12:g.(?_ 87262561)_(8767494 4_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,262,561 | 87,674,944 |
| essv7015412 | Remapped | Perfect | NC_000002.12:g.(?_ 87320178)_(8801147 1_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,320,178 | 88,011,471 |
| essv7015423 | Remapped | Perfect | NC_000002.12:g.(?_ 87437776)_(8767494 4_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,437,776 | 87,674,944 |
| essv7015434 | Remapped | Perfect | NC_000002.12:g.(?_ 87437776)_(8767494 4_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,437,776 | 87,674,944 |
| essv7015445 | Remapped | Perfect | NC_000002.12:g.(?_ 87437776)_(8769685 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,437,776 | 87,696,853 |
| essv7015456 | Remapped | Perfect | NC_000002.12:g.(?_ 87437776)_(8769685 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,437,776 | 87,696,853 |
| essv7015467 | Remapped | Perfect | NC_000002.12:g.(?_ 87575098)_(8767494 4_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,575,098 | 87,674,944 |
| essv7015478 | Remapped | Perfect | NC_000002.12:g.(?_ 87578886)_(8767494 4_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,578,886 | 87,674,944 |
| essv7015489 | Remapped | Perfect | NC_000002.12:g.(?_ 87638743)_(8766106 9_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,638,743 | 87,661,069 |
| essv7015500 | Remapped | Perfect | NC_000002.12:g.(?_ 87638743)_(8766106 9_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,638,743 | 87,661,069 |
| essv7015155 | Remapped | Pass | NC_000002.11:g.(?_ 87120495)_(8802466 7_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,120,495 | 88,024,667 |
| essv7015166 | Remapped | Pass | NC_000002.11:g.(?_ 87250496)_(8799637 2_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,250,496 | 87,996,372 |
| essv7015177 | Remapped | Pass | NC_000002.11:g.(?_ 87278884)_(8799637 2_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,278,884 | 87,996,372 |
| essv7015190 | Remapped | Pass | NC_000002.11:g.(?_ 87322042)_(8805233 0_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,322,042 | 88,052,330 |
| essv7015201 | Remapped | Pass | NC_000002.11:g.(?_ 87337969)_(8802466 7_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,337,969 | 88,024,667 |
| essv7015212 | Remapped | Pass | NC_000002.11:g.(?_ 87337969)_(8805233 0_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,337,969 | 88,052,330 |
| essv7015223 | Remapped | Pass | NC_000002.11:g.(?_ 87344738)_(8799637 2_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,344,738 | 87,996,372 |
| essv7015234 | Remapped | Pass | NC_000002.11:g.(?_ 87361172)_(8797446 3_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,361,172 | 87,974,463 |
| essv7015245 | Remapped | Pass | NC_000002.11:g.(?_ 87361172)_(8797446 3_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,361,172 | 87,974,463 |
| essv7015256 | Remapped | Pass | NC_000002.11:g.(?_ 87361172)_(8797446 3_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,361,172 | 87,974,463 |
| essv7015267 | Remapped | Pass | NC_000002.11:g.(?_ 87361172)_(8799637 2_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,361,172 | 87,996,372 |
| essv7015278 | Remapped | Pass | NC_000002.11:g.(?_ 87361172)_(8799637 2_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,361,172 | 87,996,372 |
| essv7015289 | Remapped | Pass | NC_000002.11:g.(?_ 87361172)_(8799637 2_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,361,172 | 87,996,372 |
| essv7015301 | Remapped | Pass | NC_000002.11:g.(?_ 87361172)_(8805233 0_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,361,172 | 88,052,330 |
| essv7015312 | Remapped | Pass | NC_000002.11:g.(?_ 87361172)_(8805233 0_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,361,172 | 88,052,330 |
| essv7015323 | Remapped | Pass | NC_000002.11:g.(?_ 87373893)_(8797446 3_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,373,893 | 87,974,463 |
| essv7015334 | Remapped | Pass | NC_000002.11:g.(?_ 87373893)_(8799637 2_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,373,893 | 87,996,372 |
| essv7015345 | Remapped | Pass | NC_000002.11:g.(?_ 87373893)_(8799637 2_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,373,893 | 87,996,372 |
| essv7015356 | Remapped | Pass | NC_000002.11:g.(?_ 87373893)_(8799637 2_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,373,893 | 87,996,372 |
| essv7015367 | Remapped | Pass | NC_000002.11:g.(?_ 87373893)_(8805233 0_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,373,893 | 88,052,330 |
| essv7015378 | Remapped | Pass | NC_000002.11:g.(?_ 87471843)_(8802466 7_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,471,843 | 88,024,667 |
| essv7015389 | Remapped | Pass | NC_000002.11:g.(?_ 87475440)_(8799637 2_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,475,440 | 87,996,372 |
| essv7015400 | Remapped | Pass | NC_000002.11:g.(?_ 87489684)_(8797446 3_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,489,684 | 87,974,463 |
| essv7015412 | Remapped | Pass | NC_000002.11:g.(?_ 87547301)_(8831099 0_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,547,301 | 88,310,990 |
| essv7015423 | Remapped | Pass | NC_000002.11:g.(?_ 87664899)_(8797446 3_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,664,899 | 87,974,463 |
| essv7015434 | Remapped | Pass | NC_000002.11:g.(?_ 87664899)_(8797446 3_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,664,899 | 87,974,463 |
| essv7015445 | Remapped | Pass | NC_000002.11:g.(?_ 87664899)_(8799637 2_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,664,899 | 87,996,372 |
| essv7015456 | Remapped | Pass | NC_000002.11:g.(?_ 87664899)_(8799637 2_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,664,899 | 87,996,372 |
| essv7015467 | Remapped | Perfect | NC_000002.11:g.(?_ 87874617)_(8797446 3_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,874,617 | 87,974,463 |
| essv7015478 | Remapped | Perfect | NC_000002.11:g.(?_ 87878405)_(8797446 3_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,878,405 | 87,974,463 |
| essv7015489 | Remapped | Perfect | NC_000002.11:g.(?_ 87938262)_(8796058 8_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,938,262 | 87,960,588 |
| essv7015500 | Remapped | Perfect | NC_000002.11:g.(?_ 87938262)_(8796058 8_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 87,938,262 | 87,960,588 |
| essv7015155 | Submitted genomic | NC_000002.10:g.(?_ 86974006)_(8780578 2_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 86,974,006 | 87,805,782 | ||
| essv7015166 | Submitted genomic | NC_000002.10:g.(?_ 87104007)_(8777748 7_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,104,007 | 87,777,487 | ||
| essv7015177 | Submitted genomic | NC_000002.10:g.(?_ 87132395)_(8777748 7_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,132,395 | 87,777,487 | ||
| essv7015190 | Submitted genomic | NC_000002.10:g.(?_ 87175553)_(8783344 5_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,175,553 | 87,833,445 | ||
| essv7015201 | Submitted genomic | NC_000002.10:g.(?_ 87191480)_(8780578 2_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,191,480 | 87,805,782 | ||
| essv7015212 | Submitted genomic | NC_000002.10:g.(?_ 87191480)_(8783344 5_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,191,480 | 87,833,445 | ||
| essv7015223 | Submitted genomic | NC_000002.10:g.(?_ 87198249)_(8777748 7_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,198,249 | 87,777,487 | ||
| essv7015234 | Submitted genomic | NC_000002.10:g.(?_ 87214683)_(8775557 8_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,214,683 | 87,755,578 | ||
| essv7015245 | Submitted genomic | NC_000002.10:g.(?_ 87214683)_(8775557 8_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,214,683 | 87,755,578 | ||
| essv7015256 | Submitted genomic | NC_000002.10:g.(?_ 87214683)_(8775557 8_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,214,683 | 87,755,578 | ||
| essv7015267 | Submitted genomic | NC_000002.10:g.(?_ 87214683)_(8777748 7_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,214,683 | 87,777,487 | ||
| essv7015278 | Submitted genomic | NC_000002.10:g.(?_ 87214683)_(8777748 7_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,214,683 | 87,777,487 | ||
| essv7015289 | Submitted genomic | NC_000002.10:g.(?_ 87214683)_(8777748 7_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,214,683 | 87,777,487 | ||
| essv7015301 | Submitted genomic | NC_000002.10:g.(?_ 87214683)_(8783344 5_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,214,683 | 87,833,445 | ||
| essv7015312 | Submitted genomic | NC_000002.10:g.(?_ 87214683)_(8783344 5_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,214,683 | 87,833,445 | ||
| essv7015323 | Submitted genomic | NC_000002.10:g.(?_ 87227404)_(8775557 8_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,227,404 | 87,755,578 | ||
| essv7015334 | Submitted genomic | NC_000002.10:g.(?_ 87227404)_(8777748 7_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,227,404 | 87,777,487 | ||
| essv7015345 | Submitted genomic | NC_000002.10:g.(?_ 87227404)_(8777748 7_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,227,404 | 87,777,487 | ||
| essv7015356 | Submitted genomic | NC_000002.10:g.(?_ 87227404)_(8777748 7_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,227,404 | 87,777,487 | ||
| essv7015367 | Submitted genomic | NC_000002.10:g.(?_ 87227404)_(8783344 5_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,227,404 | 87,833,445 | ||
| essv7015378 | Submitted genomic | NC_000002.10:g.(?_ 87325354)_(8780578 2_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,325,354 | 87,805,782 | ||
| essv7015389 | Submitted genomic | NC_000002.10:g.(?_ 87328951)_(8777748 7_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,328,951 | 87,777,487 | ||
| essv7015400 | Submitted genomic | NC_000002.10:g.(?_ 87343195)_(8775557 8_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,343,195 | 87,755,578 | ||
| essv7015412 | Submitted genomic | NC_000002.10:g.(?_ 87400812)_(8809210 5_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,400,812 | 88,092,105 | ||
| essv7015423 | Submitted genomic | NC_000002.10:g.(?_ 87518410)_(8775557 8_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,518,410 | 87,755,578 | ||
| essv7015434 | Submitted genomic | NC_000002.10:g.(?_ 87518410)_(8775557 8_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,518,410 | 87,755,578 | ||
| essv7015445 | Submitted genomic | NC_000002.10:g.(?_ 87518410)_(8777748 7_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,518,410 | 87,777,487 | ||
| essv7015456 | Submitted genomic | NC_000002.10:g.(?_ 87518410)_(8777748 7_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,518,410 | 87,777,487 | ||
| essv7015467 | Submitted genomic | NC_000002.10:g.(?_ 87655732)_(8775557 8_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,655,732 | 87,755,578 | ||
| essv7015478 | Submitted genomic | NC_000002.10:g.(?_ 87659520)_(8775557 8_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,659,520 | 87,755,578 | ||
| essv7015489 | Submitted genomic | NC_000002.10:g.(?_ 87719377)_(8774170 3_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,719,377 | 87,741,703 | ||
| essv7015500 | Submitted genomic | NC_000002.10:g.(?_ 87719377)_(8774170 3_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 87,719,377 | 87,741,703 |