A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463384



Internal ID21120937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116523503..116545551hg38UCSC Ensembl
chr11:116394220..116416268hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3822049
hg1922049
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463384
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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