nsv6313771
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:91,462
- Description:GRCh37/hg19 2p16.3(chr2:51125057-51216518) AND not specified
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 560 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 560 SVs from 64 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6313771 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 50,897,919 | 50,989,380 |
| nsv6313771 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 51,125,057 | 51,216,518 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv17969229 | copy number loss | Multiple | Multiple | not specified | Pathogenic | ClinVar | RCV002052693.3, VCV001526674.3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17969229 | Remapped | Perfect | NC_000002.12:g.(?_ 50897919)_(5098938 0_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 50,897,919 | 50,989,380 |
| nssv17969229 | Submitted genomic | NC_000002.11:g.(?_ 51125057)_(5121651 8_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 51,125,057 | 51,216,518 |
No validation data were submitted for this variant
Clinical Assertions
| Variant Call ID | HGVS | Type | Allele Origin | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv17969229 | GRCh37: NC_000002.11:g.(?_51125057)_(51216518_?)del | copy number loss | germline | not specified | Pathogenic | ClinVar | RCV002052693.3, VCV001526674.3 |