nsv4418398
- 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:424
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 75 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 75 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4418398 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 24,988,494 | 24,988,522 | 24,988,886 | 24,988,917 |
| nsv4418398 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 25,277,423 | 25,277,451 | 25,277,815 | 25,277,846 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15715162 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15715162 | Remapped | Perfect | NC_000010.11:g.(24 988494_24988522)_( 24988886_24988917) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 24,988,494 | 24,988,522 | 24,988,886 | 24,988,917 |
| nssv15715162 | Submitted genomic | NC_000010.10:g.(25 277423_25277451)_( 25277815_25277846) del | GRCh37 (hg19) | NC_000010.10 | Chr10 | 25,277,423 | 25,277,451 | 25,277,815 | 25,277,846 |