esv2422426
- 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:87,963
- 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: 268 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 268 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 16 SVs from 3 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2422426 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 66,893,594 | 66,981,556 |
| esv2422426 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 67,185,932 | 67,273,894 |
| esv2422426 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000015.8 | Chr15 | 64,972,986 | 65,060,948 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv5161515 | deletion | ND01580 | SNP array | SNP genotyping analysis | essv5161425, essv5161339 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5161515 | Remapped | Perfect | NC_000015.10:g.(?_ 66893594)_(6698155 6_?)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 66,893,594 | 66,981,556 |
| essv5161515 | Remapped | Perfect | NC_000015.9:g.(?_6 7185932)_(67273894 _?)del | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 67,185,932 | 67,273,894 |
| essv5161515 | Submitted genomic | NC_000015.8:g.(?_6 4972986)_(65060948 _?)del | NCBI35 (hg17) | NC_000015.8 | Chr15 | 64,972,986 | 65,060,948 |