A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733480



Internal ID157146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61389851..61390696hg38UCSC Ensembl
chr20:59964907..59965752hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146839
Supporting Variants
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733480
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.06252


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