nsv6637850
- 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:491,717
- Description:GRCh37/hg19 15q12(chr15:27265912-27757627)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: 1462 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 1462 SVs from 96 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6637850 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 27,020,765 | 27,512,481 |
| nsv6637850 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 27,265,912 | 27,757,627 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18330095 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV002473827.1, VCV001808510.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18330095 | Remapped | Perfect | NC_000015.10:g.(?_ 27020765)_(2751248 1_?)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 27,020,765 | 27,512,481 |
| nssv18330095 | Submitted genomic | NC_000015.9:g.(?_2 7265912)_(27757627 _?)dup | GRCh37 (hg19) | NC_000015.9 | Chr15 | 27,265,912 | 27,757,627 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv18330095 | GRCh37: NC_000015.9:g.(?_27265912)_(27757627_?)dup | copy number gain | unknown | not provided | Uncertain significance | ClinVar | RCV002473827.1, VCV001808510.1 | 3 |