nsv4728533
- 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:60,994,662
- Description:GRCh37/hg19 Xq21.33-28(chrX:94264404-155233731)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: 90782 SVs from 111 studies. See in: genome view
Overlapping variant regions from other studies: 90758 SVs from 111 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4728533 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 95,009,405 | 156,004,066 |
| nsv4728533 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 94,264,404 | 155,233,731 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16254132 | copy number loss | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV001259012.1, VCV000979836.1 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16254132 | Remapped | Good | NC_000023.11:g.(?_ 95009405)_(1560040 66_?)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 95,009,405 | 156,004,066 |
| nssv16254132 | Submitted genomic | NC_000023.10:g.(?_ 94264404)_(1552337 31_?)del | GRCh37 (hg19) | NC_000023.10 | ChrX | 94,264,404 | 155,233,731 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16254132 | GRCh37: NC_000023.10:g.(?_94264404)_(155233731_?)del | copy number loss | germline | not provided | Pathogenic | ClinVar | RCV001259012.1, VCV000979836.1 | 1 |