A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532395



Internal ID20905756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4716031..4736362hg38UCSC Ensembl
chr20:4696677..4717008hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3820332
hg1920332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202918
Samples
Known GenesPRND, PRNT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532395
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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