nsv4729755
- 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:8,623,213
- Description:GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3 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: 39805 SVs from 129 studies. See in: genome view
Overlapping variant regions from other studies: 37701 SVs from 130 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4729755 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 47,960,674 | 56,583,886 |
| nsv4729755 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000019.9 | Chr19 | 48,463,931 | 57,095,254 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16255652 | copy number gain | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV001259944.1, VCV000980768.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16255652 | Remapped | Good | NC_000019.10:g.(?_ 47960674)_(5658388 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 47,960,674 | 56,583,886 |
| nssv16255652 | Submitted genomic | NC_000019.9:g.(?_4 8463931)_(57095254 _?)dup | GRCh37 (hg19) | NC_000019.9 | Chr19 | 48,463,931 | 57,095,254 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16255652 | GRCh37: NC_000019.9:g.(?_48463931)_(57095254_?)dup | copy number gain | germline | not provided | Pathogenic | ClinVar | RCV001259944.1, VCV000980768.1 | 3 |