nsv3112686
- 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:10,404
- 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: 215 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 215 SVs from 52 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3112686 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 20,477,649 | 20,488,052 |
| nsv3112686 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 20,488,971 | 20,499,374 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14097847 | deletion | sample380 | Oligo aCGH | Probe signal intensity | 98 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14097847 | Remapped | Perfect | NC_000016.10:g.(?_ 20477649)_(2048805 2_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 20,477,649 | 20,488,052 |
| nssv14097847 | Submitted genomic | NC_000016.9:g.(?_2 0488971)_(20499374 _?)del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 20,488,971 | 20,499,374 |