A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531113



Internal ID20904474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4667186..4730574hg38UCSC Ensembl
chr20:4647832..4711220hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3863389
hg1963389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202915
Samples
Known GenesPRND, PRNP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531113
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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