A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14298937



Internal ID22273021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61389838..61390711hg38UCSC Ensembl
chr20:59964894..59965767hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3531520
Supporting Variants
SamplesNA19239
Known GenesCDH4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14298937
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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