nsv4451304
- 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:12,750,000
- Description:GRCh37/hg19 Yp11.32-q11.221(chrY:201704-15182563)x2 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: 8782 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 8812 SVs from 70 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4451304 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 320,650 | 13,070,649 |
| nsv4451304 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000024.9 | ChrY | 201,704 | 15,182,563 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15772422 | copy number gain | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV000847611.2, VCV000686903.2 | 2 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15772422 | Remapped | Pass | NC_000024.10:g.(?_ 320650)_(13070649_ ?)dup | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 320,650 | 13,070,649 |
| nssv15772422 | Submitted genomic | NC_000024.9:g.(?_2 01704)_(15182563_? )dup | GRCh37 (hg19) | NC_000024.9 | ChrY | 201,704 | 15,182,563 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15772422 | GRCh37: NC_000024.9:g.(?_201704)_(15182563_?)dup | copy number gain | unknown | not provided | Pathogenic | ClinVar | RCV000847611.2, VCV000686903.2 | 2 |