nsv818152
- Organism: Homo sapiens
- Study:nstd64 (Wang et al. 2007)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:17,079
- Publication(s):Wang et al. 2007
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: 221 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 221 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 8 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818152 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 76,027,992 | 76,045,070 |
| nsv818152 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 76,077,143 | 76,094,221 |
| nsv818152 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000003.9 | Chr3 | 76,159,833 | 76,176,911 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1416923 | Remapped | Perfect | NC_000003.12:g.(?_ 76027992)_(7604507 0_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 76,027,992 | 76,045,070 |
| nssv1416923 | Remapped | Perfect | NC_000003.11:g.(?_ 76077143)_(7609422 1_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 76,077,143 | 76,094,221 |
| nssv1416923 | Submitted genomic | NC_000003.9:g.(?_7 6159833)_(76176911 _?)del | NCBI35 (hg17) | NC_000003.9 | Chr3 | 76,159,833 | 76,176,911 |