nsv4452346
- 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:7,383,839
- Description:GRCh37/hg19 3p24.3-24.1(chr3:19064852-26448689)x1 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: 17959 SVs from 118 studies. See in: genome view
Overlapping variant regions from other studies: 17959 SVs from 118 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4452346 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 19,023,360 | 26,407,198 |
| nsv4452346 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 19,064,852 | 26,448,689 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15772792 | copy number loss | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV000848353.2, VCV000687662.2 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15772792 | Remapped | Perfect | NC_000003.12:g.(?_ 19023360)_(2640719 8_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 19,023,360 | 26,407,198 |
| nssv15772792 | Submitted genomic | NC_000003.11:g.(?_ 19064852)_(2644868 9_?)del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 19,064,852 | 26,448,689 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15772792 | GRCh37: NC_000003.11:g.(?_19064852)_(26448689_?)del | copy number loss | unknown | not provided | Pathogenic | ClinVar | RCV000848353.2, VCV000687662.2 | 1 |