A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272659



Internal ID20839699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22126149..22126631hg38UCSC Ensembl
chr7:22165767..22166249hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568244
Supporting Variants
Samples
Known GenesRAPGEF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272659
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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