A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv50n97



Internal ID22815447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70170311..70178971hg38UCSC Ensembl
chr11:70016417..70025077hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg388661
hg198661
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154745, nsv1154746
Samples
Known GenesANO1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv50n97
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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