nsv4402455
- Organism: Homo sapiens
- Study:nstd174 (DGV Gold Standard)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:551,064
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1619 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 1619 SVs from 71 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4402455 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 138,494,324 | 138,541,548 | 139,027,693 | 139,045,387 |
| nsv4402455 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 138,213,166 | 138,260,390 | 138,746,535 | 138,764,229 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15711294 | copy number gain | Multiple | Multiple |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15711294 | Remapped | Perfect | NC_000003.12:g.(13 8494324_138541548) _(139027693_139045 387)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 138,494,324 | 138,541,548 | 139,027,693 | 139,045,387 |
| nssv15711294 | Submitted genomic | NC_000003.11:g.(13 8213166_138260390) _(138746535_138764 229)dup | GRCh37 (hg19) | NC_000003.11 | Chr3 | 138,213,166 | 138,260,390 | 138,746,535 | 138,764,229 |