nsv433247
- 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:76,214
- 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: 1757 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 1757 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 23 SVs from 9 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433247 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 39,444,668 | 39,520,881 |
| nsv433247 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 39,302,187 | 39,378,400 |
| nsv433247 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000008.9 | Chr8 | 39,421,344 | 39,497,557 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463128 | Remapped | Perfect | NC_000008.11:g.(?_ 39444668)_(3952088 1_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 39,444,668 | 39,520,881 |
| nssv463128 | Remapped | Perfect | NC_000008.10:g.(?_ 39302187)_(3937840 0_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 39,302,187 | 39,378,400 |
| nssv463128 | Submitted genomic | NC_000008.9:g.(?_3 9421344)_(39497557 _?)del | NCBI35 (hg17) | NC_000008.9 | Chr8 | 39,421,344 | 39,497,557 |