nsv433280
- 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:54,323
- 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: 3927 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 3920 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 511 SVs from 11 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433280 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 20,367,552 | 20,421,874 |
| nsv433280 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 20,572,805 | 20,627,127 |
| nsv433280 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000015.8 | Chr15 | 18,832,819 | 18,887,141 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463161 | Remapped | Perfect | NC_000015.10:g.(?_ 20367552)_(2042187 4_?)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 20,367,552 | 20,421,874 |
| nssv463161 | Remapped | Perfect | NC_000015.9:g.(?_2 0572805)_(20627127 _?)del | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 20,572,805 | 20,627,127 |
| nssv463161 | Submitted genomic | NC_000015.8:g.(?_1 8832819)_(18887141 _?)del | NCBI35 (hg17) | NC_000015.8 | Chr15 | 18,832,819 | 18,887,141 |