nsv6635870
- Organism: Homo sapiens
- Study:nstd227 (Kikas et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:16,473
- 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: 251 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 251 SVs from 47 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6635870 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 2,629,953 | 2,646,425 |
| nsv6635870 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 2,669,587 | 2,686,059 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18328665 | duplication | SNP array | Probe signal intensity |
| nssv18328666 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv18328665 | Remapped | Perfect | NC_000007.14:g.(26 29953_?)_(?_264642 5)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 2,629,953 | 2,646,425 |
| nssv18328666 | Remapped | Perfect | NC_000007.14:g.(26 29953_?)_(?_264642 5)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 2,629,953 | 2,646,425 |
| nssv18328665 | Submitted genomic | NC_000007.13:g.(26 69587_?)_(?_268605 9)dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 2,669,587 | 2,686,059 | ||
| nssv18328666 | Submitted genomic | NC_000007.13:g.(26 69587_?)_(?_268605 9)dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 2,669,587 | 2,686,059 |