nsv433339
- 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:115,881
- 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: 573 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 573 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 52 SVs from 4 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433339 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 89,423,196 | 89,539,076 |
| nsv433339 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 88,678,195 | 88,794,075 |
| nsv433339 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000023.8 | ChrX | 88,484,340 | 88,600,220 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463220 | Remapped | Perfect | NC_000023.11:g.(?_ 89423196)_(8953907 6_?)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 89,423,196 | 89,539,076 |
| nssv463220 | Remapped | Perfect | NC_000023.10:g.(?_ 88678195)_(8879407 5_?)del | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 88,678,195 | 88,794,075 |
| nssv463220 | Submitted genomic | NC_000023.8:g.(?_8 8484340)_(88600220 _?)del | NCBI35 (hg17) | NC_000023.8 | ChrX | 88,484,340 | 88,600,220 |