A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv47n97



Internal ID22815444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42940281..42955081hg38UCSC Ensembl
chr11:42961831..42976631hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3814801
hg1914801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154718, nsv1154717
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv47n97
Frequency
Sample Size131
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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