nsv433416
- 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:91,864
- 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: 1617 SVs from 88 studies. See in: genome view
Overlapping variant regions from other studies: 1617 SVs from 88 studies. See in: genome view
Overlapping variant regions from other studies: 18 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 |
---|---|---|---|---|---|---|---|---|---|
nsv433416 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 48,829,035 | 48,920,898 |
nsv433416 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 48,850,587 | 48,942,450 |
nsv433416 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000011.8 | Chr11 | 48,807,163 | 48,899,026 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv463297 | Remapped | Perfect | NC_000011.10:g.(?_ 48829035)_(4892089 8_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 48,829,035 | 48,920,898 |
nssv463297 | Remapped | Perfect | NC_000011.9:g.(?_4 8850587)_(48942450 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 48,850,587 | 48,942,450 |
nssv463297 | Submitted genomic | NC_000011.8:g.(?_4 8807163)_(48899026 _?)dup | NCBI35 (hg17) | NC_000011.8 | Chr11 | 48,807,163 | 48,899,026 |