nsv4411181
- 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:285,315
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 921 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 921 SVs from 68 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4411181 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 163,407,108 | 163,440,740 | 163,692,422 | 163,692,422 |
nsv4411181 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 163,124,896 | 163,158,528 | 163,410,210 | 163,410,210 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15733148 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15733148 | Remapped | Perfect | NC_000003.12:g.(16 3407108_163440740) _(163692422_163692 422)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 163,407,108 | 163,440,740 | 163,692,422 | 163,692,422 |
nssv15733148 | Submitted genomic | NC_000003.11:g.(16 3124896_163158528) _(163410210_163410 210)del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 163,124,896 | 163,158,528 | 163,410,210 | 163,410,210 |