nsv4427025
- 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:56,456
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 162 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 162 SVs from 36 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4427025 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 100,453,735 | 100,454,001 | 100,509,914 | 100,510,190 |
| nsv4427025 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 102,213,492 | 102,213,758 | 102,269,671 | 102,269,947 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15708484 | copy number gain | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15708484 | Remapped | Perfect | NC_000010.11:g.(10 0453735_100454001) _(100509914_100510 190)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 100,453,735 | 100,454,001 | 100,509,914 | 100,510,190 |
| nssv15708484 | Submitted genomic | NC_000010.10:g.(10 2213492_102213758) _(102269671_102269 947)dup | GRCh37 (hg19) | NC_000010.10 | Chr10 | 102,213,492 | 102,213,758 | 102,269,671 | 102,269,947 |