nsv6314181
- 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:404,121
- Description:GRCh37/hg19 17q25.3(chr17:76770309-77174429) AND not specified
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1356 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 1356 SVs from 79 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6314181 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 78,774,227 | 79,178,347 |
| nsv6314181 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 76,770,309 | 77,174,429 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv17969142 | copy number gain | Multiple | Multiple | not specified | Uncertain significance | ClinVar | RCV002052606.3, VCV001526587.3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17969142 | Remapped | Perfect | NC_000017.11:g.(?_ 78774227)_(7917834 7_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 78,774,227 | 79,178,347 |
| nssv17969142 | Submitted genomic | NC_000017.10:g.(?_ 76770309)_(7717442 9_?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 76,770,309 | 77,174,429 |
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 |
|---|---|---|---|---|---|---|---|
| nssv17969142 | GRCh37: NC_000017.10:g.(?_76770309)_(77174429_?)dup | copy number gain | germline | not specified | Uncertain significance | ClinVar | RCV002052606.3, VCV001526587.3 |