nsv7099282
- 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:67,482
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: 319 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 319 SVs from 48 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 |
---|---|---|---|---|---|---|---|---|---|
nsv7099282 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 131,131,718 | 131,199,199 |
nsv7099282 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 130,816,477 | 130,883,958 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18793034 | deletion | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18793034 | Remapped | Perfect | NC_000007.14:g.(13 1131718_?)_(?_1311 99199)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 131,131,718 | 131,199,199 |
nssv18793034 | Submitted genomic | NC_000007.13:g.(13 0816477_?)_(?_1308 83958)del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 130,816,477 | 130,883,958 |