A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1020n223



Internal ID22803988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33110371..33461460hg38UCSC Ensembl
chr11:33131917..33483006hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38351090
hg19351090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6456989, nsv6464128
Samples
Known GenesCSTF3, CSTF3-AS1, HIPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1020n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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