A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3389792



Internal ID14890073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133027467..133027855hg38UCSC Ensembl
Innerchr11:133027467..133027855hg38UCSC Ensembl
Outerchr11:133025825..133028370hg38UCSC Ensembl
chr11:132897362..132897750hg19UCSC Ensembl
Innerchr11:132897362..132897750hg19UCSC Ensembl
Outerchr11:132895720..132898265hg19UCSC Ensembl
chr11:132402572..132402960hg18UCSC Ensembl
Innerchr11:132402572..132402960hg18UCSC Ensembl
Outerchr11:132400930..132403475hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38389
hg19389
hg18389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8651803
SamplesNA19240
Known GenesOPCML
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3389792
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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