A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539154



Internal ID20912461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56465301..56471300hg38UCSC Ensembl
chr20:55040357..55046356hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203887
Samples
Known GenesRTFDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539154
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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