A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1238n223



Internal ID22804206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81185401..81195500hg38UCSC Ensembl
chr11:80896444..80906543hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3810100
hg1910100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6468111, nsv6462714
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1238n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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