A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992638



Internal ID21901981
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 StatusM
Merged Variants
Supporting Variantsnssv17554473
Samples
Known GenesKLHL6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992638
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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