nsv818074
- 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:152,452
- 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: 1356 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 1599 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 31 SVs from 11 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818074 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 97,102,441 | 97,254,892 |
| nsv818074 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 97,768,178 | 98,024,837 |
| nsv818074 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000002.9 | Chr2 | 97,190,052 | 97,483,251 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1416321 | Remapped | Pass | NC_000002.12:g.(?_ 97102441)_(9725489 2_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,102,441 | 97,254,892 |
| nssv1416321 | Remapped | Pass | NC_000002.11:g.(?_ 97768178)_(9802483 7_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 97,768,178 | 98,024,837 |
| nssv1416321 | Submitted genomic | NC_000002.9:g.(?_9 7190052)_(97483251 _?)del | NCBI35 (hg17) | NC_000002.9 | Chr2 | 97,190,052 | 97,483,251 |