nsv6314906
- 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:261,542
- Description:NC_000016.9:g.(?_75428968)_(75690509_?)del AND not provided
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1219 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 1219 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 | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6314906 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 75,395,070 | 75,656,611 |
| nsv6314906 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 75,428,968 | 75,690,509 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv17976409 | deletion | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV002239772.3, VCV001682045.3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17976409 | Remapped | Perfect | NC_000016.10:g.(?_ 75395070)_(7565661 1_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 75,395,070 | 75,656,611 |
| nssv17976409 | Submitted genomic | NC_000016.9:g.(?_7 5428968)_(75690509 _?)del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 75,428,968 | 75,690,509 |
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 |
|---|---|---|---|---|---|---|---|
| nssv17976409 | GRCh37: NC_000016.9:g.(?_75428968)_(75690509_?)del | deletion | germline | not provided | Pathogenic | ClinVar | RCV002239772.3, VCV001682045.3 |