nsv438045
- Organism: Homo sapiens
- Study:nstd20 (McCarroll et al. 2006)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI34 (hg16)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:30,070
- Publication(s):McCarroll et al. 2006
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: 359 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 359 SVs from 46 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv438045 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 20,135,591 | 20,165,660 |
| nsv438045 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 19,993,102 | 20,023,171 |
| nsv438045 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000008.8 | Chr8 | 20,003,375 | 20,033,444 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv469769 | Remapped | Perfect | NC_000008.11:g.(?_ 20135591)_(2016566 0_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 20,135,591 | 20,165,660 |
| nssv469769 | Remapped | Perfect | NC_000008.10:g.(?_ 19993102)_(2002317 1_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 19,993,102 | 20,023,171 |
| nssv469769 | Submitted genomic | NC_000008.8:g.(?_2 0003375)_(20033444 _?)del | NCBI34 (hg16) | NC_000008.8 | Chr8 | 20,003,375 | 20,033,444 |