nsv817924
- 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:67,169
- 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: 795 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 795 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 15 SVs from 7 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 |
---|---|---|---|---|---|---|---|---|---|
nsv817924 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 23,011,810 | 23,078,978 |
nsv817924 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000021.8 | Chr21 | 24,384,132 | 24,451,300 |
nsv817924 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000021.7 | Chr21 | 23,306,003 | 23,373,171 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1416419 | Remapped | Perfect | NC_000021.9:g.(?_2 3011810)_(23078978 _?)del | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 23,011,810 | 23,078,978 |
nssv1416419 | Remapped | Perfect | NC_000021.8:g.(?_2 4384132)_(24451300 _?)del | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 24,384,132 | 24,451,300 |
nssv1416419 | Submitted genomic | NC_000021.7:g.(?_2 3306003)_(23373171 _?)del | NCBI35 (hg17) | NC_000021.7 | Chr21 | 23,306,003 | 23,373,171 |