A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524663



Internal ID20898024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:418542..506050hg38UCSC Ensembl
chr20:399186..486694hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3887509
hg1987509
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202852
Samples
Known GenesCSNK2A1, RBCK1, TBC1D20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524663
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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