nsv3899208
- 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:14,620
- Description:GRCh37/hg19 10q22.2(chr10:75633630-75648249)x0 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: 157 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 157 SVs from 35 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3899208 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 73,873,872 | 73,888,491 |
| nsv3899208 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 75,633,630 | 75,648,249 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15158414 | copy number loss | Multiple | Multiple | not provided | Benign | ClinVar | RCV000737186.2, VCV000600550.2 | 0 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15158414 | Remapped | Perfect | NC_000010.11:g.(?_ 73873872)_(7388849 1_?)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 73,873,872 | 73,888,491 |
| nssv15158414 | Submitted genomic | NC_000010.10:g.(?_ 75633630)_(7564824 9_?)del | GRCh37 (hg19) | NC_000010.10 | Chr10 | 75,633,630 | 75,648,249 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15158414 | GRCh37: NC_000010.10:g.(?_75633630)_(75648249_?)del | copy number loss | unknown | not provided | Benign | ClinVar | RCV000737186.2, VCV000600550.2 | 0 |