esv2422486
- 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:162,602
- 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: 1212 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 1216 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 42 SVs from 7 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2422486 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 11,512,989 | 11,675,590 |
| esv2422486 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 11,512,989 | 11,675,590 |
| esv2422486 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000009.9 | Chr9 | 11,502,989 | 11,665,590 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5161480 | Remapped | Perfect | NC_000009.12:g.(?_ 11512989)_(1167559 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 11,512,989 | 11,675,590 |
| essv5161480 | Remapped | Perfect | NC_000009.11:g.(?_ 11512989)_(1167559 0_?)del | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 11,512,989 | 11,675,590 |
| essv5161480 | Submitted genomic | NC_000009.9:g.(?_1 1502989)_(11665590 _?)del | NCBI35 (hg17) | NC_000009.9 | Chr9 | 11,502,989 | 11,665,590 |