nsv4728187
- 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:5,522,775
- Description:GRCh37/hg19 1p36.33-36.31(chr1:1-5592835)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: 24153 SVs from 130 studies. See in: genome view
Overlapping variant regions from other studies: 24136 SVs from 130 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4728187 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 10,001 | 5,532,775 |
| nsv4728187 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 1 | 5,592,835 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16255736 | copy number loss | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV001260116.1, VCV000980940.1 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16255736 | Remapped | Good | NC_000001.11:g.(?_ 10001)_(5532775_?) del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 10,001 | 5,532,775 |
| nssv16255736 | Submitted genomic | NC_000001.10:g.(?_ 1)_(5592835_?)del | GRCh37 (hg19) | NC_000001.10 | Chr1 | 1 | 5,592,835 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16255736 | GRCh37: NC_000001.10:g.(?_1)_(5592835_?)del | copy number loss | germline | not provided | Pathogenic | ClinVar | RCV001260116.1, VCV000980940.1 | 1 |