nsv3112721
- 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:8,582
- 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: 251 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 251 SVs from 46 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 |
---|---|---|---|---|---|---|---|---|---|
nsv3112721 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 82,369,676 | 82,378,257 |
nsv3112721 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 80,327,552 | 80,336,133 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv14098884 | deletion | sample138 | Oligo aCGH | Probe signal intensity | 112 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14098884 | Remapped | Perfect | NC_000017.11:g.(?_ 82369676)_(8237825 7_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 82,369,676 | 82,378,257 |
nssv14098884 | Submitted genomic | NC_000017.10:g.(?_ 80327552)_(8033613 3_?)del | GRCh37 (hg19) | NC_000017.10 | Chr17 | 80,327,552 | 80,336,133 |