A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799337



Internal ID19180533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:79083057..79089126hg38UCSC Ensembl
Innerchr11:78794102..78800171hg19UCSC Ensembl
Innerchr11:78471750..78477819hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg386070
hg196070
hg186070
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892028
Supporting Variants
Samples
Known GenesTENM4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799337
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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