nsv6314855
- 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:2,145
- Description:NC_000009.11:g.(?_34370797)_(34372941_?)dup 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: 114 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 120 SVs from 25 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6314855 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 34,370,799 | 34,372,943 |
| nsv6314855 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 34,370,797 | 34,372,941 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv17976398 | duplication | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV002238800.3, VCV001681161.3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17976398 | Remapped | Perfect | NC_000009.12:g.(?_ 34370799)_(3437294 3_?)dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 34,370,799 | 34,372,943 |
| nssv17976398 | Submitted genomic | NC_000009.11:g.(?_ 34370797)_(3437294 1_?)dup | GRCh37 (hg19) | NC_000009.11 | Chr9 | 34,370,797 | 34,372,941 |
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 |
|---|---|---|---|---|---|---|---|
| nssv17976398 | GRCh37: NC_000009.11:g.(?_34370797)_(34372941_?)dup | duplication | germline | not provided | Uncertain significance | ClinVar | RCV002238800.3, VCV001681161.3 |