nsv4410222
- 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:137,238
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 402 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 402 SVs from 56 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4410222 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 31,663,706 | 31,663,706 | 31,800,943 | 31,800,943 |
nsv4410222 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 31,888,775 | 31,888,775 | 32,026,012 | 32,026,012 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15727796 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15727796 | Remapped | Perfect | NC_000002.12:g.(31 663706_31663706)_( 31800943_31800943) del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 31,663,706 | 31,663,706 | 31,800,943 | 31,800,943 |
nssv15727796 | Submitted genomic | NC_000002.11:g.(31 888775_31888775)_( 32026012_32026012) del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 31,888,775 | 31,888,775 | 32,026,012 | 32,026,012 |