esv2422237
- Organism: Homo sapiens
- Study:estd196 (Simon-Sanchez et al. 2006)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:607,017
- Publication(s):Simon-Sanchez et al. 2006
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: 1542 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 1542 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 84 SVs from 6 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2422237 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 90,180,785 | 90,787,801 |
| esv2422237 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 91,940,542 | 92,547,558 |
| esv2422237 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000010.8 | Chr10 | 91,930,522 | 92,537,538 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv5161280 | duplication | ND01566 | SNP array | SNP genotyping analysis | essv5161462 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5161280 | Remapped | Perfect | NC_000010.11:g.(?_ 90180785)_(9078780 1_?)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 90,180,785 | 90,787,801 |
| essv5161280 | Remapped | Perfect | NC_000010.10:g.(?_ 91940542)_(9254755 8_?)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 91,940,542 | 92,547,558 |
| essv5161280 | Submitted genomic | NC_000010.8:g.(?_9 1930522)_(92537538 _?)dup | NCBI35 (hg17) | NC_000010.8 | Chr10 | 91,930,522 | 92,537,538 |