nsv4412627
- 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:49,763
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 408 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 416 SVs from 72 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4412627 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 155,211,057 | 155,213,823 | 155,248,181 | 155,260,819 |
| nsv4412627 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 155,180,848 | 155,183,614 | 155,217,972 | 155,230,610 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15714859 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15714859 | Remapped | Perfect | NC_000001.11:g.(15 5211057_155213823) _(155248181_155260 819)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 155,211,057 | 155,213,823 | 155,248,181 | 155,260,819 |
| nssv15714859 | Submitted genomic | NC_000001.10:g.(15 5180848_155183614) _(155217972_155230 610)del | GRCh37 (hg19) | NC_000001.10 | Chr1 | 155,180,848 | 155,183,614 | 155,217,972 | 155,230,610 |