nsv3113961
- Organism: Homo sapiens
- Study:nstd145 (Lu et al. 2017)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:146,529
- Publication(s):Lu et al. 2017
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: 718 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 718 SVs from 62 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3113961 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 138,931,457 | 139,077,985 |
| nsv3113961 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 138,013,619 | 138,160,147 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14101779 | duplication | sample363 | Oligo aCGH | Probe signal intensity | 100 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14101779 | Remapped | Perfect | NC_000023.11:g.(?_ 138931457)_(139077 985_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 138,931,457 | 139,077,985 |
| nssv14101779 | Submitted genomic | NC_000023.10:g.(?_ 138013619)_(138160 147_?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 138,013,619 | 138,160,147 |