nsv5673880
- 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:1,130
- Description:NC_000009.11:g.(?_129376729)_(129377858_?)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: 78 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 78 SVs from 27 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv5673880 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 126,614,450 | 126,615,579 |
| nsv5673880 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 129,376,729 | 129,377,858 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv17172871 | deletion | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV001384891.1, VCV001072237.1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17172871 | Remapped | Perfect | NC_000009.12:g.(?_ 126614450)_(126615 579_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 126,614,450 | 126,615,579 |
| nssv17172871 | Submitted genomic | NC_000009.11:g.(?_ 129376729)_(129377 858_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 129,376,729 | 129,377,858 |
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 |
|---|---|---|---|---|---|---|---|
| nssv17172871 | GRCh37: NC_000009.11:g.(?_129376729)_(129377858_?)del | deletion | germline | not provided | Pathogenic | ClinVar | RCV001384891.1, VCV001072237.1 |