nsv433463
- 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:97,968
- 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: 624 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 557 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 40 SVs from 8 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433463 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 140,958,435 | 141,056,402 |
| nsv433463 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 140,084,056 | 140,150,590 |
| nsv433463 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000023.8 | ChrX | 139,766,120 | 139,876,110 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463344 | Remapped | Pass | NC_000023.11:g.(?_ 140958435)_(141056 402_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 140,958,435 | 141,056,402 |
| nssv463344 | Remapped | Pass | NC_000023.10:g.(?_ 140084056)_(140150 590_?)dup | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 140,084,056 | 140,150,590 |
| nssv463344 | Submitted genomic | NC_000023.8:g.(?_1 39766120)_(1398761 10_?)dup | NCBI35 (hg17) | NC_000023.8 | ChrX | 139,766,120 | 139,876,110 |