nsv4411803
- 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:309,722
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1585 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 1585 SVs from 93 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4411803 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 8,844,447 | 8,882,095 | 9,135,287 | 9,154,168 |
nsv4411803 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 8,884,077 | 8,921,725 | 9,174,917 | 9,193,798 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15739930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15739930 | Remapped | Perfect | NC_000007.14:g.(88 44447_8882095)_(91 35287_9154168)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 8,844,447 | 8,882,095 | 9,135,287 | 9,154,168 |
nssv15739930 | Submitted genomic | NC_000007.13:g.(88 84077_8921725)_(91 74917_9193798)del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 8,884,077 | 8,921,725 | 9,174,917 | 9,193,798 |