A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933660



Internal ID23173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44722641..44722732hg38UCSC Ensembl
chr3:44764133..44764224hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436015
Supporting Variants
Samples
Known GenesZNF502
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933660
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.021386


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