nsv3908757
- 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:339,835
- Description:GRCh37/hg19 10q21.3(chr10:68254082-68593916)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: 2535 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 2535 SVs from 86 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3908757 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 66,494,324 | 66,834,158 |
| nsv3908757 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 68,254,082 | 68,593,916 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15170858 | copy number loss | Multiple | Multiple | not provided | Benign | ClinVar | RCV000749666.2, VCV000613030.2 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15170858 | Remapped | Perfect | NC_000010.11:g.(?_ 66494324)_(6683415 8_?)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 66,494,324 | 66,834,158 |
| nssv15170858 | Submitted genomic | NC_000010.10:g.(?_ 68254082)_(6859391 6_?)del | GRCh37 (hg19) | NC_000010.10 | Chr10 | 68,254,082 | 68,593,916 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15170858 | GRCh37: NC_000010.10:g.(?_68254082)_(68593916_?)del | copy number loss | unknown | not provided | Benign | ClinVar | RCV000749666.2, VCV000613030.2 | 1 |