nsv6635795
- Organism: Homo sapiens
- Study:nstd227 (Kikas et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:286,095
- Publication(s):Kikas et al. 2023
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: 1349 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1349 SVs from 84 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6635795 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 100,598,177 | 100,884,271 |
| nsv6635795 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 101,138,382 | 101,424,476 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18327543 | duplication | SNP array | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18327543 | Remapped | Perfect | NC_000015.10:g.(10 0598177_?)_(?_1008 84271)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 100,598,177 | 100,884,271 |
| nssv18327543 | Submitted genomic | NC_000015.9:g.(101 138382_?)_(?_10142 4476)dup | GRCh37 (hg19) | NC_000015.9 | Chr15 | 101,138,382 | 101,424,476 |