A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892088



Internal ID19186484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99438277..99466563hg38UCSC Ensembl
Outerchr11:99438277..99466563hg38UCSC Ensembl
Innerchr11:99309008..99337294hg19UCSC Ensembl
Outerchr11:99309008..99337294hg19UCSC Ensembl
Innerchr11:98814218..98842504hg18UCSC Ensembl
Outerchr11:98814218..98842504hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3828287
hg1928287
hg1828287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798492
Samples
Known GenesCNTN5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892088
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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