nsv4398726
- 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:382,271
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1053 SVs from 66 studies. See in: genome view
Overlapping variant regions from other studies: 1053 SVs from 66 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4398726 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 106,081,902 | 106,151,302 | 106,455,665 | 106,464,172 |
| nsv4398726 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 106,529,777 | 106,599,177 | 106,903,540 | 106,912,047 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15712284 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15712284 | Remapped | Perfect | NC_000006.12:g.(10 6081902_106151302) _(106455665_106464 172)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 106,081,902 | 106,151,302 | 106,455,665 | 106,464,172 |
| nssv15712284 | Submitted genomic | NC_000006.11:g.(10 6529777_106599177) _(106903540_106912 047)dup | GRCh37 (hg19) | NC_000006.11 | Chr6 | 106,529,777 | 106,599,177 | 106,903,540 | 106,912,047 |