nsv4674785
- 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:19,097,455
- Description:GRCh37/hg19 1q41-43(chr1:219916966-239004378)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: 49451 SVs from 134 studies. See in: genome view
Overlapping variant regions from other studies: 49450 SVs from 134 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4674785 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 219,743,624 | 238,841,078 |
| nsv4674785 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 219,916,966 | 239,004,378 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16206530 | copy number gain | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV001005175.1, VCV000814163.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16206530 | Remapped | Good | NC_000001.11:g.(?_ 219743624)_(238841 078_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 219,743,624 | 238,841,078 |
| nssv16206530 | Submitted genomic | NC_000001.10:g.(?_ 219916966)_(239004 378_?)dup | GRCh37 (hg19) | NC_000001.10 | Chr1 | 219,916,966 | 239,004,378 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16206530 | GRCh37: NC_000001.10:g.(?_219916966)_(239004378_?)dup | copy number gain | germline | not provided | Pathogenic | ClinVar | RCV001005175.1, VCV000814163.1 | 3 |