A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735326



Internal ID158992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11792444..11856168hg38UCSC Ensembl
chr5:11792556..11856280hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3863725
hg1963725
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459613
Supporting Variants
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735326
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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