A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892097



Internal ID18839807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106829320..106858946hg38UCSC Ensembl
Outerchr11:106814355..106858946hg38UCSC Ensembl
Innerchr11:106700046..106729672hg19UCSC Ensembl
Outerchr11:106685081..106729672hg19UCSC Ensembl
Innerchr11:106205256..106234882hg18UCSC Ensembl
Outerchr11:106190291..106234882hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3844592
hg1944592
hg1844592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786489, essv25786786
Samples
Known GenesGUCY1A2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892097
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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