A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732334



Internal ID156000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38870497..38871309hg38UCSC Ensembl
chr20:37499140..37499952hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521712
Supporting Variants
Samples
Known GenesPPP1R16B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732334
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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