nsv3115193
- 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:378,028
- 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: 1667 SVs from 91 studies. See in: genome view
Overlapping variant regions from other studies: 1667 SVs from 91 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3115193 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 19,072,487 | 19,450,514 |
| nsv3115193 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000005.9 | Chr5 | 19,072,596 | 19,450,623 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14109208 | deletion | sample274 | Oligo aCGH | Probe signal intensity | 73 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14109208 | Remapped | Perfect | NC_000005.10:g.(?_ 19072487)_(1945051 4_?)del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 19,072,487 | 19,450,514 |
| nssv14109208 | Submitted genomic | NC_000005.9:g.(?_1 9072596)_(19450623 _?)del | GRCh37 (hg19) | NC_000005.9 | Chr5 | 19,072,596 | 19,450,623 |