A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966018



Internal ID44668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55569962..55569962hg38UCSC Ensembl
chr5:54865790..54865790hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544161
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966018
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.602398


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