A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1208n223



Internal ID22804176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63418601..63431400hg38UCSC Ensembl
chr11:63186073..63198872hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3812800
hg1912800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6456753, nsv6465652, nsv6468838
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1208n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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