nsv4404358
- 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:124,550
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 853 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 833 SVs from 77 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4404358 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 144,105,310 | 144,105,310 | 144,229,859 | 144,229,859 |
| nsv4404358 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 145,160,213 | 145,160,213 | 145,284,762 | 145,284,762 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15713129 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15713129 | Remapped | Perfect | NC_000008.11:g.(14 4105310_144105310) _(144229859_144229 859)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 144,105,310 | 144,105,310 | 144,229,859 | 144,229,859 |
| nssv15713129 | Submitted genomic | NC_000008.10:g.(14 5160213_145160213) _(145284762_145284 762)dup | GRCh37 (hg19) | NC_000008.10 | Chr8 | 145,160,213 | 145,160,213 | 145,284,762 | 145,284,762 |