A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998217



Internal ID7081620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99620679..99631191hg38UCSC Ensembl
Innerchr11:99491410..99501922hg19UCSC Ensembl
Innerchr11:98996620..99007132hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3810513
hg1910513
hg1810513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586205
SamplesHuRef
Known GenesCNTN5
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998217
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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