nsv4455332
- 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:3,969,200
- Description:GRCh37/hg19 11q25(chr11:130969272-134938470)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: 12941 SVs from 118 studies. See in: genome view
Overlapping variant regions from other studies: 12942 SVs from 118 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4455332 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 131,099,377 | 135,068,576 |
| nsv4455332 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 130,969,272 | 134,938,470 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15776136 | copy number loss | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV000848686.2, VCV000687995.2 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15776136 | Remapped | Perfect | NC_000011.10:g.(?_ 131099377)_(135068 576_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 131,099,377 | 135,068,576 |
| nssv15776136 | Submitted genomic | NC_000011.9:g.(?_1 30969272)_(1349384 70_?)del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 130,969,272 | 134,938,470 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15776136 | GRCh37: NC_000011.9:g.(?_130969272)_(134938470_?)del | copy number loss | unknown | not provided | Pathogenic | ClinVar | RCV000848686.2, VCV000687995.2 | 1 |