nsv933295
- 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:193,235
- 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: 1282 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 1283 SVs from 54 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv933295 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 31,786,342 | 31,979,576 |
| nsv933295 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 31,804,459 | 31,997,693 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv1615561 | deletion | 2962 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv1615561 | Remapped | Perfect | NC_000023.11:g.(31 774421_31786342)_( 31979576_31989336) del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 31,774,421 | 31,786,342 | 31,979,576 | 31,989,336 |
| nssv1615561 | Submitted genomic | NC_000023.10:g.(31 792538_31804459)_( 31997693_32007453) del | GRCh37 (hg19) | NC_000023.10 | ChrX | 31,792,538 | 31,804,459 | 31,997,693 | 32,007,453 |