nsv4401367
- 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:288,481
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1138 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 1138 SVs from 77 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4401367 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 15,294,410 | 15,295,808 | 15,559,329 | 15,582,890 |
nsv4401367 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 15,334,035 | 15,335,433 | 15,598,954 | 15,622,515 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15740039 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15740039 | Remapped | Perfect | NC_000007.14:g.(15 294410_15295808)_( 15559329_15582890) del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 15,294,410 | 15,295,808 | 15,559,329 | 15,582,890 |
nssv15740039 | Submitted genomic | NC_000007.13:g.(15 334035_15335433)_( 15598954_15622515) del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 15,334,035 | 15,335,433 | 15,598,954 | 15,622,515 |