A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673268



Internal ID9939373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4779901..4889350hg38UCSC Ensembl
chr11:4801131..4910580hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38109450
hg19109450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5511764
SamplesNA20807
Known GenesOR51F2, OR51S1, OR51T1, OR52R1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673268
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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