A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893627



Internal ID18837761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3063890..3069774hg38UCSC Ensembl
Outerchr3:3063890..3069774hg38UCSC Ensembl
Innerchr3:3105574..3111458hg19UCSC Ensembl
Outerchr3:3105574..3111458hg19UCSC Ensembl
Innerchr3:3080574..3086458hg18UCSC Ensembl
Outerchr3:3080574..3086458hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg385885
hg195885
hg185885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799799
Samples
Known GenesIL5RA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893627
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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