A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891905



Internal ID18839615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:269147..336332hg38UCSC Ensembl
Outerchr11:269147..336332hg38UCSC Ensembl
Innerchr11:269147..336332hg19UCSC Ensembl
Outerchr11:269147..336332hg19UCSC Ensembl
Innerchr11:259147..326332hg18UCSC Ensembl
Outerchr11:259147..326332hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3867186
hg1967186
hg1867186
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788996
Samples
Known GenesATHL1, IFITM1, IFITM2, IFITM3, IFITM5, NLRP6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891905
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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