nsv7097789
- 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:4,194
- Description:NC_000008.10:g.(?_145664016)_(145668209_?)dup 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: 362 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 359 SVs from 40 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv7097789 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 144,438,633 | 144,442,826 |
| nsv7097789 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 145,664,016 | 145,668,209 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv18790808 | duplication | Multiple | Multiple | not provided | Likely pathogenic | ClinVar | RCV003116660.2, VCV002425866.2 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18790808 | Remapped | Perfect | NC_000008.11:g.(?_ 144438633)_(144442 826_?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 144,438,633 | 144,442,826 |
| nssv18790808 | Submitted genomic | NC_000008.10:g.(?_ 145664016)_(145668 209_?)dup | GRCh37 (hg19) | NC_000008.10 | Chr8 | 145,664,016 | 145,668,209 |
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 |
|---|---|---|---|---|---|---|---|
| nssv18790808 | GRCh37: NC_000008.10:g.(?_145664016)_(145668209_?)dup | duplication | germline | not provided | Likely pathogenic | ClinVar | RCV003116660.2, VCV002425866.2 |