nsv4397307
- 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:532,199
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1383 SVs from 82 studies. See in: genome view
Overlapping variant regions from other studies: 1383 SVs from 82 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4397307 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 93,105,978 | 93,170,714 | 93,589,685 | 93,638,176 |
nsv4397307 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 94,027,129 | 94,091,865 | 94,510,836 | 94,559,327 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15734599 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15734599 | Remapped | Perfect | NC_000004.12:g.(93 105978_93170714)_( 93589685_93638176) del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 93,105,978 | 93,170,714 | 93,589,685 | 93,638,176 |
nssv15734599 | Submitted genomic | NC_000004.11:g.(94 027129_94091865)_( 94510836_94559327) del | GRCh37 (hg19) | NC_000004.11 | Chr4 | 94,027,129 | 94,091,865 | 94,510,836 | 94,559,327 |