nsv3921598
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37, GRCh38, NCBI36
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:137,922,077
- Description:GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3 AND See cases
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 326145 SVs from 149 studies. See in: genome view
Overlapping variant regions from other studies: 326168 SVs from 149 studies. See in: genome view
Overlapping variant regions from other studies: 82536 SVs from 42 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nsv3921598 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 203,861 | 138,125,937 |
| nsv3921598 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 203,861 | 141,020,389 |
| nsv3921598 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 193,861 | 140,140,210 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15148176 | copy number gain | Multiple | Multiple | See cases | Pathogenic | ClinVar | RCV000141876.6, VCV000153518.2 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nssv15148176 | Submitted genomic | NC_000009.12:g.(?_ 203861)_(138125937 _?)dup | GRCh38 (hg38) | NC_000009.12 | Chr9 | 203,861 | 138,125,937 |
| nssv15148176 | Submitted genomic | NC_000009.11:g.(?_ 203861)_(141020389 _?)dup | GRCh37 (hg19) | NC_000009.11 | Chr9 | 203,861 | 141,020,389 |
| nssv15148176 | Submitted genomic | NC_000009.10:g.(?_ 193861)_(140140210 _?)dup | NCBI36 (hg18) | NC_000009.10 | Chr9 | 193,861 | 140,140,210 |
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 | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15148176 | GRCh37: NC_000009.11:g.(?_203861)_(141020389_?)dup, GRCh38: NC_000009.12:g.(?_203861)_(138125937_?)dup, NCBI36: NC_000009.10:g.(?_193861)_(140140210_?)dup | copy number gain | not provided | See cases | Pathogenic | ClinVar | RCV000141876.6, VCV000153518.2 | 3 |