A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14299920



Internal ID22302112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34716848..34718903hg38UCSC Ensembl
chr20:33304652..33306707hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382056
hg192056
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226179
Supporting Variants
SamplesNA19240
Known GenesNCOA6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14299920
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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