A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17554473



Internal ID21878828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183490621..183490715hg38UCSC Ensembl
chr3:183208409..183208503hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992638
Supporting Variants
Samples
Known GenesKLHL6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17554473
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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