A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465487



Internal ID21123040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116716184..116801139hg38UCSC Ensembl
chr11:116586900..116671855hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3884956
hg1984956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987105
Samples
Known GenesAPOA5, BUD13, ZNF259
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465487
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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