nsv481832
- Organism: Homo sapiens
- Study:nstd36 (Mitsui et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:338,800
- Publication(s):Mitsui et al. 2010
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1502 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 1503 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 353 SVs from 17 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv481832 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 31,760,577 | 32,099,376 |
| nsv481832 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 31,778,694 | 32,117,493 |
| nsv481832 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 31,688,615 | 32,027,414 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation |
|---|---|---|---|---|---|---|
| nssv650112 | deletion | Oligo aCGH, Sequencing | Probe signal intensity, Sequence alignment | Muscular Dystrophy, Duchenne | Pathogenic | Submitter |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv650112 | Remapped | Perfect | NC_000023.11:g.317 60577_32099376del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 31,760,577 | 32,099,376 |
| nssv650112 | Remapped | Perfect | NC_000023.10:g.317 78694_32117493del | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 31,778,694 | 32,117,493 |
| nssv650112 | Submitted genomic | NC_000023.9:g.3168 8615_32027414del | NCBI36 (hg18) | NC_000023.9 | ChrX | 31,688,615 | 32,027,414 |
No validation data were submitted for this variant
Clinical Assertions
| Variant Call ID | HGVS | Type | Subject Phenotype | Clinical Interpretation | Source of Interpretation |
|---|---|---|---|---|---|
| nssv650112 | NCBI36: NC_000023.9:g.31688615_32027414del | deletion | Muscular Dystrophy, Duchenne | Pathogenic | Submitter |