A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786775



Internal ID19164105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:79113278..79180160hg38UCSC Ensembl
Innerchr11:78824323..78891205hg19UCSC Ensembl
Innerchr11:78501971..78568853hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3866883
hg1966883
hg1866883
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892029
Supporting Variants
Samples
Known GenesTENM4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=29
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786775
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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