nsv6313935
- 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:2,277,706
- Description:GRCh37/hg19 9q34.3(chr9:138740078-141020389) 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: 11210 SVs from 119 studies. See in: genome view
Overlapping variant regions from other studies: 11126 SVs from 119 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6313935 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 135,848,232 | 138,125,937 |
| nsv6313935 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 138,740,078 | 141,020,389 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv17969386 | copy number loss | Multiple | Multiple | not specified | Pathogenic | ClinVar | RCV002052850.3, VCV001527564.3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17969386 | Remapped | Good | NC_000009.12:g.(?_ 135848232)_(138125 937_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 135,848,232 | 138,125,937 |
| nssv17969386 | Submitted genomic | NC_000009.11:g.(?_ 138740078)_(141020 389_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 138,740,078 | 141,020,389 |
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 |
|---|---|---|---|---|---|---|---|
| nssv17969386 | GRCh37: NC_000009.11:g.(?_138740078)_(141020389_?)del | copy number loss | germline | not specified | Pathogenic | ClinVar | RCV002052850.3, VCV001527564.3 |