nsv4405670
- 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:486,731
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 780 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 780 SVs from 75 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4405670 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 95,247,530 | 95,339,583 | 95,682,571 | 95,734,260 |
| nsv4405670 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 95,913,278 | 96,005,331 | 96,348,319 | 96,400,008 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15710557 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15710557 | Remapped | Perfect | NC_000002.12:g.(95 247530_95339583)_( 95682571_95734260) dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 95,247,530 | 95,339,583 | 95,682,571 | 95,734,260 |
| nssv15710557 | Submitted genomic | NC_000002.11:g.(95 913278_96005331)_( 96348319_96400008) dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 95,913,278 | 96,005,331 | 96,348,319 | 96,400,008 |