A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666330



Internal ID9932435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55654858..55836170hg38UCSC Ensembl
chr11:55422334..55603646hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38181313
hg19181313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv212e199
Supporting Variantsessv5896112, essv6078253, essv5793185, essv6227679
SamplesNA19239, NA19225, HG01375, NA19093
Known GenesOR4C6, OR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666330
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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