A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965164



Internal ID44092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24574743..24574743hg38UCSC Ensembl
chr5:24574852..24574852hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551243
Supporting Variants
Samples
Known GenesCDH10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965164
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.354961


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