nsv6635958
- 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:202,563
- 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: 2899 SVs from 104 studies. See in: genome view
Overlapping variant regions from other studies: 3091 SVs from 104 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6635958 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 19,745,778 | 19,948,340 |
| nsv6635958 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 20,213,937 | 20,416,499 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18327367 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv18327367 | Remapped | Perfect | NC_000014.9:g.(197 45778_?)_(?_199483 40)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 19,745,778 | 19,948,340 |
| nssv18327367 | Submitted genomic | NC_000014.8:g.(202 13937_?)_(?_204164 99)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 20,213,937 | 20,416,499 |