nsv933531
- Organism: Homo sapiens
- Study:nstd80 (Boone et al. 2013)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:465,883
- Publication(s):Boone et al. 2013
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: 1796 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 1797 SVs from 69 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv933531 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 31,647,836 | 32,113,718 |
| nsv933531 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 31,665,953 | 32,131,835 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv1616611 | deletion | 3010 | Oligo aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv1616611 | Remapped | Perfect | NC_000023.11:g.(31 637920_31647836)_( 32113718_32123978) del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 31,637,920 | 31,647,836 | 32,113,718 | 32,123,978 |
| nssv1616611 | Submitted genomic | NC_000023.10:g.(31 656037_31665953)_( 32131835_32142095) del | GRCh37 (hg19) | NC_000023.10 | ChrX | 31,656,037 | 31,665,953 | 32,131,835 | 32,142,095 |