nsv3111677
- 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:26,738
- 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: 383 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 383 SVs from 57 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3111677 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 44,273,233 | 44,299,970 |
| nsv3111677 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 44,500,372 | 44,527,109 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14105161 | deletion | sample262 | Oligo aCGH | Probe signal intensity | 74 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14105161 | Remapped | Perfect | NC_000002.12:g.(?_ 44273233)_(4429997 0_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 44,273,233 | 44,299,970 |
| nssv14105161 | Submitted genomic | NC_000002.11:g.(?_ 44500372)_(4452710 9_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 44,500,372 | 44,527,109 |