nsv4400300
- 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:407,451
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1499 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1499 SVs from 84 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4400300 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 150,743,286 | 150,753,961 | 151,149,833 | 151,150,736 |
nsv4400300 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 151,664,438 | 151,675,113 | 152,070,985 | 152,071,888 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15711612 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15711612 | Remapped | Perfect | NC_000004.12:g.(15 0743286_150753961) _(151149833_151150 736)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 150,743,286 | 150,753,961 | 151,149,833 | 151,150,736 |
nssv15711612 | Submitted genomic | NC_000004.11:g.(15 1664438_151675113) _(152070985_152071 888)dup | GRCh37 (hg19) | NC_000004.11 | Chr4 | 151,664,438 | 151,675,113 | 152,070,985 | 152,071,888 |