nsv3116646
- 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:342,979
- 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: 984 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 984 SVs from 68 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3116646 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 80,589,826 | 80,932,804 |
| nsv3116646 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 81,510,980 | 81,853,958 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14107108 | deletion | sample1 | Oligo aCGH | Probe signal intensity | 77 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14107108 | Remapped | Perfect | NC_000004.12:g.(?_ 80589826)_(8093280 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 80,589,826 | 80,932,804 |
| nssv14107108 | Submitted genomic | NC_000004.11:g.(?_ 81510980)_(8185395 8_?)del | GRCh37 (hg19) | NC_000004.11 | Chr4 | 81,510,980 | 81,853,958 |