nsv433341
- 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:100,263
- 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: 471 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 471 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 50 SVs from 6 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433341 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 91,844,386 | 91,944,648 |
| nsv433341 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 91,099,385 | 91,199,647 |
| nsv433341 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000023.8 | ChrX | 90,905,530 | 91,005,792 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463222 | Remapped | Perfect | NC_000023.11:g.(?_ 91844386)_(9194464 8_?)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 91,844,386 | 91,944,648 |
| nssv463222 | Remapped | Perfect | NC_000023.10:g.(?_ 91099385)_(9119964 7_?)del | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 91,099,385 | 91,199,647 |
| nssv463222 | Submitted genomic | NC_000023.8:g.(?_9 0905530)_(91005792 _?)del | NCBI35 (hg17) | NC_000023.8 | ChrX | 90,905,530 | 91,005,792 |