A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696738



Internal ID120404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64543844..64553510hg38UCSC Ensembl
chr14:65010562..65020228hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg389667
hg199667
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513249
Supporting Variants
Samples
Known GenesPPP1R36
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696738
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001249


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