nsv3117026
- 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:4,653
- 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: 186 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 186 SVs from 49 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3117026 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 47,915,523 | 47,920,175 |
| nsv3117026 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 48,207,720 | 48,212,372 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14096110 | Remapped | Perfect | NC_000015.10:g.(?_ 47915523)_(4792017 5_?)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 47,915,523 | 47,920,175 |
| nssv14098130 | Remapped | Perfect | NC_000015.10:g.(?_ 47915523)_(4792017 5_?)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 47,915,523 | 47,920,175 |
| nssv14096110 | Submitted genomic | NC_000015.9:g.(?_4 8207720)_(48212372 _?)del | GRCh37 (hg19) | NC_000015.9 | Chr15 | 48,207,720 | 48,212,372 | ||
| nssv14098130 | Submitted genomic | NC_000015.9:g.(?_4 8207720)_(48212372 _?)del | GRCh37 (hg19) | NC_000015.9 | Chr15 | 48,207,720 | 48,212,372 |