A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891919



Internal ID19186315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5539196..5587044hg38UCSC Ensembl
Outerchr11:5539196..5587044hg38UCSC Ensembl
Innerchr11:5560426..5608274hg19UCSC Ensembl
Outerchr11:5560426..5608274hg19UCSC Ensembl
Innerchr11:5517002..5564850hg18UCSC Ensembl
Outerchr11:5517002..5564850hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3847849
hg1947849
hg1847849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782876
Samples
Known GenesOR52B6, OR52H1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891919
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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