A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv51n97



Internal ID22815448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86174680..86191421hg38UCSC Ensembl
chr11:85885722..85902463hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3816742
hg1916742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154753, nsv1154754
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv51n97
Frequency
Sample Size131
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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