nsv4421838
- 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:469,656
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1916 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 1949 SVs from 93 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4421838 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 43,322,294 | 43,322,294 | 43,791,949 | 43,791,949 |
| nsv4421838 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 41,399,657 | 41,411,555 | 41,760,909 | 41,869,317 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15709911 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15709911 | Remapped | Good | NC_000017.11:g.(43 322294_43322294)_( 43791949_43791949) dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 43,322,294 | 43,322,294 | 43,791,949 | 43,791,949 |
| nssv15709911 | Submitted genomic | NC_000017.10:g.(41 399657_41411555)_( 41760909_41869317) dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 41,399,657 | 41,411,555 | 41,760,909 | 41,869,317 |