A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8651792



Internal ID15099633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119938084..119938486hg38UCSC Ensembl
Innerchr11:119938084..119938486hg38UCSC Ensembl
Outerchr11:119937718..119938562hg38UCSC Ensembl
chr11:119808793..119809195hg19UCSC Ensembl
Innerchr11:119808793..119809195hg19UCSC Ensembl
Outerchr11:119808427..119809271hg19UCSC Ensembl
chr11:119314003..119314405hg18UCSC Ensembl
Innerchr11:119314003..119314405hg18UCSC Ensembl
Outerchr11:119313637..119314481hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38403
hg19403
hg18403
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3348842
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8651792
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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