A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8953640



Internal ID14159165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81572822..81572836hg38UCSC Ensembl
Innerchr11:81572813..81572845hg38UCSC Ensembl
Outerchr11:81572799..81572859hg38UCSC Ensembl
chr11:81283864..81283878hg19UCSC Ensembl
Innerchr11:81283855..81283887hg19UCSC Ensembl
Outerchr11:81283841..81283901hg19UCSC Ensembl
chr11:80961512..80961526hg18UCSC Ensembl
Innerchr11:80961535..80961503hg18UCSC Ensembl
Outerchr11:80961489..80961549hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3370860
Supporting Variants
SamplesNA18571
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8953640
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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