nsv4413154
- 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:78,283
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 499 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 497 SVs from 60 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4413154 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 80,653 | 81,306 | 138,448 | 158,935 |
| nsv4413154 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000020.10 | Chr20 | 61,294 | 61,947 | 119,089 | 139,576 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15710774 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15710774 | Remapped | Perfect | NC_000020.11:g.(80 653_81306)_(138448 _158935)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 80,653 | 81,306 | 138,448 | 158,935 |
| nssv15710774 | Submitted genomic | NC_000020.10:g.(61 294_61947)_(119089 _139576)dup | GRCh37 (hg19) | NC_000020.10 | Chr20 | 61,294 | 61,947 | 119,089 | 139,576 |