nsv4426506
- 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:32,784
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 202 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 207 SVs from 49 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4426506 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 21,601,896 | 21,601,896 | 21,634,679 | 21,634,679 |
| nsv4426506 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 22,070,046 | 22,070,046 | 22,102,823 | 22,102,835 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15721317 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15721317 | Remapped | Good | NC_000014.9:g.(216 01896_21601896)_(2 1634679_21634679)d el | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 21,601,896 | 21,601,896 | 21,634,679 | 21,634,679 |
| nssv15721317 | Submitted genomic | NC_000014.8:g.(220 70046_22070046)_(2 2102823_22102835)d el | GRCh37 (hg19) | NC_000014.8 | Chr14 | 22,070,046 | 22,070,046 | 22,102,823 | 22,102,835 |