nsv4429662
- 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:320
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 113 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 113 SVs from 34 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4429662 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 99,052,437 | 99,052,446 | 99,052,751 | 99,052,756 |
| nsv4429662 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 99,446,215 | 99,446,224 | 99,446,529 | 99,446,534 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15719785 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15719785 | Remapped | Perfect | NC_000012.12:g.(99 052437_99052446)_( 99052751_99052756) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 99,052,437 | 99,052,446 | 99,052,751 | 99,052,756 |
| nssv15719785 | Submitted genomic | NC_000012.11:g.(99 446215_99446224)_( 99446529_99446534) del | GRCh37 (hg19) | NC_000012.11 | Chr12 | 99,446,215 | 99,446,224 | 99,446,529 | 99,446,534 |