nsv817720
- 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:62,474
- 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: 284 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 284 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 9 SVs from 4 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv817720 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 7,865,053 | 7,927,526 |
| nsv817720 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 7,915,055 | 7,977,528 |
| nsv817720 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000016.8 | Chr16 | 7,855,056 | 7,917,529 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1417073 | Remapped | Perfect | NC_000016.10:g.(?_ 7865053)_(7927526_ ?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 7,865,053 | 7,927,526 |
| nssv1417073 | Remapped | Perfect | NC_000016.9:g.(?_7 915055)_(7977528_? )del | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 7,915,055 | 7,977,528 |
| nssv1417073 | Submitted genomic | NC_000016.8:g.(?_7 855056)_(7917529_? )del | NCBI35 (hg17) | NC_000016.8 | Chr16 | 7,855,056 | 7,917,529 |