nsv4729665
- 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:926,112
- Description:GRCh37/hg19 11p15.5(chr11:230615-1150353)x3 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: 7152 SVs from 106 studies. See in: genome view
Overlapping variant regions from other studies: 6907 SVs from 106 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4729665 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 230,615 | 1,156,726 |
| nsv4729665 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 230,615 | 1,150,353 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16254419 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV001259592.1, VCV000980416.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16254419 | Remapped | Good | NC_000011.10:g.(?_ 230615)_(1156726_? )dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 230,615 | 1,156,726 |
| nssv16254419 | Submitted genomic | NC_000011.9:g.(?_2 30615)_(1150353_?) dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 230,615 | 1,150,353 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16254419 | GRCh37: NC_000011.9:g.(?_230615)_(1150353_?)dup | copy number gain | germline | not provided | Uncertain significance | ClinVar | RCV001259592.1, VCV000980416.1 | 3 |