nsv433257
- Organism: Homo sapiens
- Study:nstd14 (Cooper et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:58,739
- Publication(s):Cooper et al. 2008
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: 608 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 612 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 23 SVs from 4 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433257 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 11,359,656 | 11,418,394 |
| nsv433257 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 11,359,656 | 11,418,394 |
| nsv433257 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000009.9 | Chr9 | 11,349,656 | 11,408,394 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463138 | Remapped | Perfect | NC_000009.12:g.(?_ 11359656)_(1141839 4_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 11,359,656 | 11,418,394 |
| nssv463138 | Remapped | Perfect | NC_000009.11:g.(?_ 11359656)_(1141839 4_?)del | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 11,359,656 | 11,418,394 |
| nssv463138 | Submitted genomic | NC_000009.9:g.(?_1 1349656)_(11408394 _?)del | NCBI35 (hg17) | NC_000009.9 | Chr9 | 11,349,656 | 11,408,394 |