nsv433321
- 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:47,459
- 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: 502 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 502 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 11 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433321 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 46,755,299 | 46,802,757 |
| nsv433321 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 46,796,789 | 46,844,247 |
| nsv433321 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000003.9 | Chr3 | 46,771,793 | 46,819,251 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463202 | Remapped | Perfect | NC_000003.12:g.(?_ 46755299)_(4680275 7_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 46,755,299 | 46,802,757 |
| nssv463202 | Remapped | Perfect | NC_000003.11:g.(?_ 46796789)_(4684424 7_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 46,796,789 | 46,844,247 |
| nssv463202 | Submitted genomic | NC_000003.9:g.(?_4 6771793)_(46819251 _?)del | NCBI35 (hg17) | NC_000003.9 | Chr3 | 46,771,793 | 46,819,251 |