A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799799



Internal ID18813130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3063890..3069774hg38UCSC Ensembl
Innerchr3:3105574..3111458hg19UCSC Ensembl
Innerchr3:3080574..3086458hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg385885
hg195885
hg185885
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893627
Supporting Variants
Samples
Known GenesIL5RA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799799
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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