A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14165469



Internal ID5862610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55691646..55841751hg38UCSC Ensembl
chr11:55459122..55609227hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38150106
hg19150106
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626453
Supporting Variants
SamplesNA19239
Known GenesOR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14165469
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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