nsv4410174
- 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:113,538
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 485 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 485 SVs from 63 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4410174 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 109,591,382 | 109,605,409 | 109,684,308 | 109,704,919 |
| nsv4410174 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 110,348,959 | 110,362,986 | 110,441,885 | 110,462,496 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15710604 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15710604 | Remapped | Perfect | NC_000002.12:g.(10 9591382_109605409) _(109684308_109704 919)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 109,591,382 | 109,605,409 | 109,684,308 | 109,704,919 |
| nssv15710604 | Submitted genomic | NC_000002.11:g.(11 0348959_110362986) _(110441885_110462 496)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 110,348,959 | 110,362,986 | 110,441,885 | 110,462,496 |