nsv4413532
- 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:594,915
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1711 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 1711 SVs from 79 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4413532 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 100,906,404 | 100,952,525 | 101,396,284 | 101,501,318 |
| nsv4413532 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 101,372,741 | 101,418,862 | 101,862,621 | 101,967,655 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15707562 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15707562 | Remapped | Perfect | NC_000014.9:g.(100 906404_100952525)_ (101396284_1015013 18)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 100,906,404 | 100,952,525 | 101,396,284 | 101,501,318 |
| nssv15707562 | Submitted genomic | NC_000014.8:g.(101 372741_101418862)_ (101862621_1019676 55)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 101,372,741 | 101,418,862 | 101,862,621 | 101,967,655 |