A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890742



Internal ID19185044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:134474110..134487387hg38UCSC Ensembl
Outerchr5:134474110..134487387hg38UCSC Ensembl
Innerchr5:133809801..133823078hg19UCSC Ensembl
Outerchr5:133809801..133823078hg19UCSC Ensembl
Innerchr5:133837700..133850977hg18UCSC Ensembl
Outerchr5:133837700..133850977hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3813278
hg1913278
hg1813278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786989
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890742
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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