nsv6634747
- 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:127,968
- 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: 928 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 928 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6634747 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 162,370,911 | 162,498,878 |
| nsv6634747 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 162,088,699 | 162,216,666 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18328255 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv18328255 | Remapped | Perfect | NC_000003.12:g.(16 2370911_?)_(?_1624 98878)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 162,370,911 | 162,498,878 |
| nssv18328255 | Submitted genomic | NC_000003.11:g.(16 2088699_?)_(?_1622 16666)dup | GRCh37 (hg19) | NC_000003.11 | Chr3 | 162,088,699 | 162,216,666 |