A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892069



Internal ID18839779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94211379..94296722hg38UCSC Ensembl
Outerchr11:94211379..94316021hg38UCSC Ensembl
Innerchr11:93944545..94029888hg19UCSC Ensembl
Outerchr11:93944545..94049187hg19UCSC Ensembl
Innerchr11:93584193..93669536hg18UCSC Ensembl
Outerchr11:93584193..93688835hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38104643
hg19104643
hg18104643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796916, essv25796540, essv25797442, essv25797511
Samples
Known GenesFOLR4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892069
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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