nsv4412986
- 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:76,490
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 398 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 398 SVs from 56 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4412986 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 66,413,661 | 66,414,465 | 66,489,304 | 66,490,150 |
| nsv4412986 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 64,409,779 | 64,410,583 | 64,485,422 | 64,486,268 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15725206 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15725206 | Remapped | Perfect | NC_000017.11:g.(66 413661_66414465)_( 66489304_66490150) del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 66,413,661 | 66,414,465 | 66,489,304 | 66,490,150 |
| nssv15725206 | Submitted genomic | NC_000017.10:g.(64 409779_64410583)_( 64485422_64486268) del | GRCh37 (hg19) | NC_000017.10 | Chr17 | 64,409,779 | 64,410,583 | 64,485,422 | 64,486,268 |