nsv6636905
- 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:1,431,678
- Description:GRCh37/hg19 Xq22.3(chrX:105730612-107162289)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: 1858 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 1858 SVs from 67 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6636905 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 106,487,382 | 107,919,059 |
| nsv6636905 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 105,730,612 | 107,162,289 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18330098 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV002473830.1, VCV001808513.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18330098 | Remapped | Perfect | NC_000023.11:g.(?_ 106487382)_(107919 059_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 106,487,382 | 107,919,059 |
| nssv18330098 | Submitted genomic | NC_000023.10:g.(?_ 105730612)_(107162 289_?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 105,730,612 | 107,162,289 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv18330098 | GRCh37: NC_000023.10:g.(?_105730612)_(107162289_?)dup | copy number gain | unknown | not provided | Uncertain significance | ClinVar | RCV002473830.1, VCV001808513.1 | 3 |