nsv4728473
- 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:407,617
- Description:GRCh37/hg19 Xq28(chrX:148448248-148855992)x4 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: 731 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 725 SVs from 70 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4728473 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 149,366,718 | 149,774,334 |
| nsv4728473 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 148,448,248 | 148,855,992 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16254614 | copy number gain | Multiple | Multiple | not provided | Likely benign | ClinVar | RCV001260056.1, VCV000980880.1 | 4 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16254614 | Remapped | Good | NC_000023.11:g.(?_ 149366718)_(149774 334_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 149,366,718 | 149,774,334 |
| nssv16254614 | Submitted genomic | NC_000023.10:g.(?_ 148448248)_(148855 992_?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 148,448,248 | 148,855,992 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16254614 | GRCh37: NC_000023.10:g.(?_148448248)_(148855992_?)dup | copy number gain | germline | not provided | Likely benign | ClinVar | RCV001260056.1, VCV000980880.1 | 4 |