nsv818943
- 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:90,942
- 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: 1041 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 1041 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 38 SVs from 10 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818943 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 131,345,787 | 131,436,728 |
| nsv818943 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 131,830,332 | 131,921,273 |
| nsv818943 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000012.9 | Chr12 | 130,355,212 | 130,446,153 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1417127 | Remapped | Perfect | NC_000012.12:g.(?_ 131345787)_(131436 728_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 131,345,787 | 131,436,728 |
| nssv1417127 | Remapped | Perfect | NC_000012.11:g.(?_ 131830332)_(131921 273_?)dup | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 131,830,332 | 131,921,273 |
| nssv1417127 | Submitted genomic | NC_000012.9:g.(?_1 30355212)_(1304461 53_?)dup | NCBI35 (hg17) | NC_000012.9 | Chr12 | 130,355,212 | 130,446,153 |