nsv3906087
- 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:201,657
- Description:GRCh37/hg19 11p12(chr11:40453077-40654733)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: 554 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 554 SVs from 62 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3906087 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 40,431,527 | 40,633,183 |
| nsv3906087 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 40,453,077 | 40,654,733 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15153842 | copy number loss | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV000683316.1, VCV000563827.1 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15153842 | Remapped | Perfect | NC_000011.10:g.(?_ 40431527)_(4063318 3_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 40,431,527 | 40,633,183 |
| nssv15153842 | Submitted genomic | NC_000011.9:g.(?_4 0453077)_(40654733 _?)del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 40,453,077 | 40,654,733 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15153842 | GRCh37: NC_000011.9:g.(?_40453077)_(40654733_?)del | copy number loss | germline | not provided | Uncertain significance | ClinVar | RCV000683316.1, VCV000563827.1 | 1 |