A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193938



Internal ID20760978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114225467..114248290hg38UCSC Ensembl
chr13:114990942..115013765hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3822824
hg1922824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492235
Supporting Variants
Samples
Known GenesCDC16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193938
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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