A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520899



Internal ID20894260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3858619..3859462hg38UCSC Ensembl
chr20:3839266..3840109hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38844
hg19844
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202245
Samples
Known GenesMAVS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520899
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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