nsv4423400
- 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:202,297
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 954 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 954 SVs from 83 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4423400 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 4,366,254 | 4,374,608 | 4,542,518 | 4,568,550 |
| nsv4423400 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 4,387,484 | 4,395,838 | 4,563,748 | 4,589,780 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15717363 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15717363 | Remapped | Perfect | NC_000011.10:g.(43 66254_4374608)_(45 42518_4568550)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 4,366,254 | 4,374,608 | 4,542,518 | 4,568,550 |
| nssv15717363 | Submitted genomic | NC_000011.9:g.(438 7484_4395838)_(456 3748_4589780)del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 4,387,484 | 4,395,838 | 4,563,748 | 4,589,780 |