nsv6635895
- 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:289,671
- 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: 979 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 979 SVs from 85 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 |
---|---|---|---|---|---|---|---|---|---|
nsv6635895 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 110,736,271 | 111,025,941 |
nsv6635895 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 110,376,327 | 110,665,997 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18328735 | deletion | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18328735 | Remapped | Perfect | NC_000007.14:g.(11 0736271_?)_(?_1110 25941)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 110,736,271 | 111,025,941 |
nssv18328735 | Submitted genomic | NC_000007.13:g.(11 0376327_?)_(?_1106 65997)del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 110,376,327 | 110,665,997 |