nsv7099209
- 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:46,427
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: 243 SVs from 33 studies. See in: genome view
Overlapping variant regions from other studies: 243 SVs from 33 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 |
---|---|---|---|---|---|---|---|---|---|
nsv7099209 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 61,101,976 | 61,148,402 |
nsv7099209 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 61,567,648 | 61,614,074 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18793016 | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18793016 | Remapped | Perfect | NC_000001.11:g.(61 101976_?)_(?_61148 402)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 61,101,976 | 61,148,402 |
nssv18793016 | Submitted genomic | NC_000001.10:g.(61 567648_?)_(?_61614 074)dup | GRCh37 (hg19) | NC_000001.10 | Chr1 | 61,567,648 | 61,614,074 |