nsv818318
- 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:128,330
- 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: 673 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 673 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 36 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818318 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 13,204,437 | 13,332,766 |
| nsv818318 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 13,204,549 | 13,332,878 |
| nsv818318 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000005.8 | Chr5 | 13,257,549 | 13,385,878 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1417461 | Remapped | Perfect | NC_000005.10:g.(?_ 13204437)_(1333276 6_?)del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 13,204,437 | 13,332,766 |
| nssv1417461 | Remapped | Perfect | NC_000005.9:g.(?_1 3204549)_(13332878 _?)del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 13,204,549 | 13,332,878 |
| nssv1417461 | Submitted genomic | NC_000005.8:g.(?_1 3257549)_(13385878 _?)del | NCBI35 (hg17) | NC_000005.8 | Chr5 | 13,257,549 | 13,385,878 |