nsv4407165
- 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:64
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 91 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 91 SVs from 20 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4407165 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 45,977,334 | 45,977,342 | 45,977,395 | 45,977,397 |
| nsv4407165 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 46,018,826 | 46,018,834 | 46,018,887 | 46,018,889 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15732199 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15732199 | Remapped | Perfect | NC_000003.12:g.(45 977334_45977342)_( 45977395_45977397) del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 45,977,334 | 45,977,342 | 45,977,395 | 45,977,397 |
| nssv15732199 | Submitted genomic | NC_000003.11:g.(46 018826_46018834)_( 46018887_46018889) del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 46,018,826 | 46,018,834 | 46,018,887 | 46,018,889 |