nsv4395997
- 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:99,847
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 591 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 593 SVs from 74 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4395997 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 87,575,098 | 87,584,639 | 87,673,102 | 87,674,944 |
| nsv4395997 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 87,874,617 | 87,884,158 | 87,972,621 | 87,974,463 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15728368 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15728368 | Remapped | Perfect | NC_000002.12:g.(87 575098_87584639)_( 87673102_87674944) del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 87,575,098 | 87,584,639 | 87,673,102 | 87,674,944 |
| nssv15728368 | Submitted genomic | NC_000002.11:g.(87 874617_87884158)_( 87972621_87974463) del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 87,874,617 | 87,884,158 | 87,972,621 | 87,974,463 |