nsv433260
- 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:50,775
- 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: 376 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 376 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 14 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433260 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 55,462,023 | 55,512,797 |
| nsv433260 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 57,221,783 | 57,272,557 |
| nsv433260 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000010.8 | Chr10 | 56,891,789 | 56,942,563 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463141 | Remapped | Perfect | NC_000010.11:g.(?_ 55462023)_(5551279 7_?)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 55,462,023 | 55,512,797 |
| nssv463141 | Remapped | Perfect | NC_000010.10:g.(?_ 57221783)_(5727255 7_?)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 57,221,783 | 57,272,557 |
| nssv463141 | Submitted genomic | NC_000010.8:g.(?_5 6891789)_(56942563 _?)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 56,891,789 | 56,942,563 |