nsv433236
- 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:60,549
- 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: 2574 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 2574 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 731 SVs from 14 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433236 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 78,263,213 | 78,323,761 |
| nsv433236 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 78,972,930 | 79,033,478 |
| nsv433236 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000006.9 | Chr6 | 79,029,649 | 79,090,197 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463117 | Remapped | Perfect | NC_000006.12:g.(?_ 78263213)_(7832376 1_?)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 78,263,213 | 78,323,761 |
| nssv463117 | Remapped | Perfect | NC_000006.11:g.(?_ 78972930)_(7903347 8_?)del | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 78,972,930 | 79,033,478 |
| nssv463117 | Submitted genomic | NC_000006.9:g.(?_7 9029649)_(79090197 _?)del | NCBI35 (hg17) | NC_000006.9 | Chr6 | 79,029,649 | 79,090,197 |