A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3426898



Internal ID14927169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133377614..133377627hg38UCSC Ensembl
Innerchr11:133377616..133377625hg38UCSC Ensembl
Outerchr11:133377612..133377629hg38UCSC Ensembl
chr11:133247509..133247522hg19UCSC Ensembl
Innerchr11:133247511..133247520hg19UCSC Ensembl
Outerchr11:133247507..133247524hg19UCSC Ensembl
chr11:132752719..132752732hg18UCSC Ensembl
Innerchr11:132752721..132752730hg18UCSC Ensembl
Outerchr11:132752717..132752734hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865544
SamplesNA12005
Known GenesOPCML
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3426898
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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