A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5511764



Internal ID9911291
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 Flag1
Merged StatusS
Merged Variantsesv2673268
Supporting Variants
SamplesNA20807
Known GenesOR51F2, OR51S1, OR51T1, OR52R1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5511764
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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