nsv3117469
- Organism: Homo sapiens
- Study:nstd145 (Lu et al. 2017)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:6,168
- 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: 149 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 149 SVs from 35 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 |
---|---|---|---|---|---|---|---|---|---|
nsv3117469 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 33,780,470 | 33,786,637 |
nsv3117469 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 32,107,489 | 32,113,656 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14098002 | Remapped | Perfect | NC_000017.11:g.(?_ 33780470)_(3378663 7_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 33,780,470 | 33,786,637 |
nssv14098909 | Remapped | Perfect | NC_000017.11:g.(?_ 33780470)_(3378663 7_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 33,780,470 | 33,786,637 |
nssv14098002 | Submitted genomic | NC_000017.10:g.(?_ 32107489)_(3211365 6_?)del | GRCh37 (hg19) | NC_000017.10 | Chr17 | 32,107,489 | 32,113,656 | ||
nssv14098909 | Submitted genomic | NC_000017.10:g.(?_ 32107489)_(3211365 6_?)del | GRCh37 (hg19) | NC_000017.10 | Chr17 | 32,107,489 | 32,113,656 |