nsv4399516
- 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:38,000
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 172 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 172 SVs from 42 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4399516 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 46,975,211 | 46,975,211 | 47,013,210 | 47,013,210 |
| nsv4399516 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 47,016,701 | 47,016,701 | 47,054,700 | 47,054,700 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15732210 | copy number loss | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15732210 | Remapped | Perfect | NC_000003.12:g.(46 975211_46975211)_( 47013210_47013210) del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 46,975,211 | 46,975,211 | 47,013,210 | 47,013,210 |
| nssv15732210 | Submitted genomic | NC_000003.11:g.(47 016701_47016701)_( 47054700_47054700) del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 47,016,701 | 47,016,701 | 47,054,700 | 47,054,700 |