A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469824



Internal ID21127377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73759901..73761500hg38UCSC Ensembl
chr11:73470946..73472545hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182467
Samples
Known GenesRAB6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469824
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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