A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791333



Internal ID19178723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87546857..87664609hg38UCSC Ensembl
Innerchr11:87257749..87375501hg19UCSC Ensembl
Innerchr11:86935397..87053149hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38117753
hg19117753
hg18117753
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892050
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=21
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791333
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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