A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534581



Internal ID20907942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3841015..3851868hg38UCSC Ensembl
chr20:3821662..3832515hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3810854
hg1910854
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202240
Samples
Known GenesMAVS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534581
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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