nsv3111576
- 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:5,943
- 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: 615 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 615 SVs from 78 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3111576 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 5,763,604 | 5,769,546 |
| nsv3111576 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 5,784,834 | 5,790,776 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14091067 | Remapped | Perfect | NC_000011.10:g.(?_ 5763604)_(5769546_ ?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 5,763,604 | 5,769,546 |
| nssv14091743 | Remapped | Perfect | NC_000011.10:g.(?_ 5763604)_(5769546_ ?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 5,763,604 | 5,769,546 |
| nssv14091067 | Submitted genomic | NC_000011.9:g.(?_5 784834)_(5790776_? )del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 5,784,834 | 5,790,776 | ||
| nssv14091743 | Submitted genomic | NC_000011.9:g.(?_5 784834)_(5790776_? )del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 5,784,834 | 5,790,776 |