A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463725



Internal ID21121278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78915327..79052635hg38UCSC Ensembl
chr11:78626372..78763680hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38137309
hg19137309
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194618
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463725
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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