nsv4673891
- 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:12,731,058
- Description:GRCh37/hg19 Xq24-26.1(chrX:117119895-129850963)x2 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: 20348 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 20349 SVs from 95 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4673891 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 117,985,932 | 130,716,989 |
| nsv4673891 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 117,119,895 | 129,850,963 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16208640 | copy number gain | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV001007336.1, VCV000816382.1 | 2 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16208640 | Remapped | Perfect | NC_000023.11:g.(?_ 117985932)_(130716 989_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 117,985,932 | 130,716,989 |
| nssv16208640 | Submitted genomic | NC_000023.10:g.(?_ 117119895)_(129850 963_?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 117,119,895 | 129,850,963 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16208640 | GRCh37: NC_000023.10:g.(?_117119895)_(129850963_?)dup | copy number gain | germline | not provided | Pathogenic | ClinVar | RCV001007336.1, VCV000816382.1 | 2 |