A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659046



Internal ID9925151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69281650..69288870hg38UCSC Ensembl
chr11:69049117..69056337hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg387221
hg197221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6529322
SamplesNA19448
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659046
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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