nsv6637670
- 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:2,736,282
- Description:GRCh37/hg19 8q21.13-21.2(chr8:83705217-86441492)x1 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: 7049 SVs from 113 studies. See in: genome view
Overlapping variant regions from other studies: 7060 SVs from 113 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6637670 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 82,792,982 | 85,529,263 |
| nsv6637670 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 83,705,217 | 86,441,492 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18329132 | copy number loss | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV002475586.1, VCV001809213.1 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18329132 | Remapped | Perfect | NC_000008.11:g.(?_ 82792982)_(8552926 3_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 82,792,982 | 85,529,263 |
| nssv18329132 | Submitted genomic | NC_000008.10:g.(?_ 83705217)_(8644149 2_?)del | GRCh37 (hg19) | NC_000008.10 | Chr8 | 83,705,217 | 86,441,492 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv18329132 | GRCh37: NC_000008.10:g.(?_83705217)_(86441492_?)del | copy number loss | unknown | not provided | Uncertain significance | ClinVar | RCV002475586.1, VCV001809213.1 | 1 |