nsv4413788
- 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:302,993
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1009 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 1009 SVs from 83 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4413788 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 55,679,434 | 55,702,735 | 55,970,800 | 55,982,426 |
nsv4413788 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 57,439,194 | 57,462,495 | 57,730,560 | 57,742,186 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15716447 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15716447 | Remapped | Perfect | NC_000010.11:g.(55 679434_55702735)_( 55970800_55982426) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 55,679,434 | 55,702,735 | 55,970,800 | 55,982,426 |
nssv15716447 | Submitted genomic | NC_000010.10:g.(57 439194_57462495)_( 57730560_57742186) del | GRCh37 (hg19) | NC_000010.10 | Chr10 | 57,439,194 | 57,462,495 | 57,730,560 | 57,742,186 |