nsv4400464
- 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:2,379
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 403 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 403 SVs from 35 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4400464 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 169,723,100 | 169,723,385 | 169,725,322 | 169,725,478 |
| nsv4400464 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 170,123,196 | 170,123,481 | 170,125,418 | 170,125,574 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15739647 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15739647 | Remapped | Perfect | NC_000006.12:g.(16 9723100_169723385) _(169725322_169725 478)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 169,723,100 | 169,723,385 | 169,725,322 | 169,725,478 |
| nssv15739647 | Submitted genomic | NC_000006.11:g.(17 0123196_170123481) _(170125418_170125 574)del | GRCh37 (hg19) | NC_000006.11 | Chr6 | 170,123,196 | 170,123,481 | 170,125,418 | 170,125,574 |