nsv7099236
- Organism: Homo sapiens
- Study:nstd231 (Ali 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:1,739,954
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: 4048 SVs from 91 studies. See in: genome view
Overlapping variant regions from other studies: 4055 SVs from 91 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv7099236 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 156,064,931 | 157,804,884 |
| nsv7099236 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 156,034,722 | 157,774,674 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18792969 | duplication | SNP array | SNP genotyping analysis |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18792969 | Remapped | Perfect | NC_000001.11:g.(15 6064931_?)_(?_1578 04884)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 156,064,931 | 157,804,884 |
| nssv18792969 | Submitted genomic | NC_000001.10:g.(15 6034722_?)_(?_1577 74674)dup | GRCh37 (hg19) | NC_000001.10 | Chr1 | 156,034,722 | 157,774,674 |