A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792776



Internal ID18828597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4240025..4355975hg38UCSC Ensembl
Innerchr11:4261255..4377205hg19UCSC Ensembl
Innerchr11:4217831..4333781hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38115951
hg19115951
hg18115951
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891912
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792776
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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