nsv6635074
- 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:126,456
- 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: 2029 SVs from 105 studies. See in: genome view
Overlapping variant regions from other studies: 2029 SVs from 105 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6635074 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 133,438,843 | 133,565,298 |
| nsv6635074 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 135,252,347 | 135,378,802 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18327057 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv18327057 | Remapped | Perfect | NC_000010.11:g.(13 3438843_?)_(?_1335 65298)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 133,438,843 | 133,565,298 |
| nssv18327057 | Submitted genomic | NC_000010.10:g.(13 5252347_?)_(?_1353 78802)dup | GRCh37 (hg19) | NC_000010.10 | Chr10 | 135,252,347 | 135,378,802 |