A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3375309



Internal ID15222284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114314211..114314230hg38UCSC Ensembl
Innerchr11:114314207..114314234hg38UCSC Ensembl
Outerchr11:114314188..114314253hg38UCSC Ensembl
chr11:114184933..114184952hg19UCSC Ensembl
Innerchr11:114184929..114184956hg19UCSC Ensembl
Outerchr11:114184910..114184975hg19UCSC Ensembl
chr11:113690143..113690162hg18UCSC Ensembl
Innerchr11:113690166..113690139hg18UCSC Ensembl
Outerchr11:113690120..113690185hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9654536
SamplesNA19143
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3375309
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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