nsv4451577
- 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:205,728
- Description:GRCh37/hg19 Xq28(chrX:153609873-153815499)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: 536 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 539 SVs from 63 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4451577 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 154,381,513 | 154,587,240 |
| nsv4451577 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 153,609,873 | 153,815,499 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15775601 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV000847592.2, VCV000686884.2 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15775601 | Remapped | Good | NC_000023.11:g.(?_ 154381513)_(154587 240_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 154,381,513 | 154,587,240 |
| nssv15775601 | Submitted genomic | NC_000023.10:g.(?_ 153609873)_(153815 499_?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 153,609,873 | 153,815,499 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15775601 | GRCh37: NC_000023.10:g.(?_153609873)_(153815499_?)dup | copy number gain | unknown | not provided | Uncertain significance | ClinVar | RCV000847592.2, VCV000686884.2 | 3 |