nsv4393584
- 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:15,126
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 138 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 138 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4393584 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 81,234,410 | 81,234,410 | 81,249,528 | 81,249,535 |
| nsv4393584 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000005.9 | Chr5 | 80,530,229 | 80,530,229 | 80,545,347 | 80,545,354 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15736403 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15736403 | Remapped | Perfect | NC_000005.10:g.(81 234410_81234410)_( 81249528_81249535) del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 81,234,410 | 81,234,410 | 81,249,528 | 81,249,535 |
| nssv15736403 | Submitted genomic | NC_000005.9:g.(805 30229_80530229)_(8 0545347_80545354)d el | GRCh37 (hg19) | NC_000005.9 | Chr5 | 80,530,229 | 80,530,229 | 80,545,347 | 80,545,354 |