nsv433340
- 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:89,500
- 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: 488 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 488 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 48 SVs from 5 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433340 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 91,489,439 | 91,578,938 |
| nsv433340 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 90,744,438 | 90,833,937 |
| nsv433340 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000023.8 | ChrX | 90,550,583 | 90,640,082 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463221 | Remapped | Perfect | NC_000023.11:g.(?_ 91489439)_(9157893 8_?)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 91,489,439 | 91,578,938 |
| nssv463221 | Remapped | Perfect | NC_000023.10:g.(?_ 90744438)_(9083393 7_?)del | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 90,744,438 | 90,833,937 |
| nssv463221 | Submitted genomic | NC_000023.8:g.(?_9 0550583)_(90640082 _?)del | NCBI35 (hg17) | NC_000023.8 | ChrX | 90,550,583 | 90,640,082 |