A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234996



Internal ID20802036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:256601..384500hg38UCSC Ensembl
chr6:256601..384500hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38127900
hg19127900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399088
Supporting Variants
Samples
Known GenesDUSP22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234996
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.66214


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