A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460411



Internal ID21117964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63427801..63436700hg38UCSC Ensembl
chr11:63195273..63204172hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178233
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460411
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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