nsv4457495
- 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:543,305
- Description:GRCh37/hg19 17q25.3(chr17:79663313-80197463)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: 2136 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 2116 SVs from 85 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4457495 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 81,696,283 | 82,239,587 |
| nsv4457495 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 79,663,313 | 80,197,463 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15775916 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV000848219.2, VCV000687520.2 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15775916 | Remapped | Good | NC_000017.11:g.(?_ 81696283)_(8223958 7_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 81,696,283 | 82,239,587 |
| nssv15775916 | Submitted genomic | NC_000017.10:g.(?_ 79663313)_(8019746 3_?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 79,663,313 | 80,197,463 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15775916 | GRCh37: NC_000017.10:g.(?_79663313)_(80197463_?)dup | copy number gain | unknown | not provided | Uncertain significance | ClinVar | RCV000848219.2, VCV000687520.2 | 3 |