A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892101



Internal ID18839811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:111208771..111269737hg38UCSC Ensembl
Outerchr11:111208771..111269737hg38UCSC Ensembl
Innerchr11:111079495..111140462hg19UCSC Ensembl
Outerchr11:111079495..111140462hg19UCSC Ensembl
Innerchr11:110584705..110645672hg18UCSC Ensembl
Outerchr11:110584705..110645672hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3860967
hg1960968
hg1860968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797243
Samples
Known GenesC11orf53
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892101
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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