A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460569



Internal ID21118122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68119301..68124100hg38UCSC Ensembl
chr11:67886768..67891567hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186853
Samples
Known GenesCHKA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460569
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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