nsv4729929
- 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:1,389,504
- Description:GRCh37/hg19 17p13.1(chr17:6650649-8040151)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: 4852 SVs from 98 studies. See in: genome view
Overlapping variant regions from other studies: 4853 SVs from 98 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4729929 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 6,747,330 | 8,136,833 |
| nsv4729929 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 6,650,649 | 8,040,151 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16254274 | copy number gain | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV001259299.1, VCV000980123.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16254274 | Remapped | Perfect | NC_000017.11:g.(?_ 6747330)_(8136833_ ?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 6,747,330 | 8,136,833 |
| nssv16254274 | Submitted genomic | NC_000017.10:g.(?_ 6650649)_(8040151_ ?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 6,650,649 | 8,040,151 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16254274 | GRCh37: NC_000017.10:g.(?_6650649)_(8040151_?)dup | copy number gain | germline | not provided | Pathogenic | ClinVar | RCV001259299.1, VCV000980123.1 | 3 |