nsv817632
- 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:118,942
- 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: 411 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 411 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 23 SVs from 5 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv817632 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 46,778,196 | 46,897,137 |
| nsv817632 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 47,247,399 | 47,366,340 |
| nsv817632 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000014.7 | Chr14 | 46,317,149 | 46,436,090 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1416395 | Remapped | Perfect | NC_000014.9:g.(?_4 6778196)_(46897137 _?)del | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 46,778,196 | 46,897,137 |
| nssv1416395 | Remapped | Perfect | NC_000014.8:g.(?_4 7247399)_(47366340 _?)del | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 47,247,399 | 47,366,340 |
| nssv1416395 | Submitted genomic | NC_000014.7:g.(?_4 6317149)_(46436090 _?)del | NCBI35 (hg17) | NC_000014.7 | Chr14 | 46,317,149 | 46,436,090 |