A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894165



Internal ID19185234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29421514..29461866hg38UCSC Ensembl
Outerchr5:29421514..29461866hg38UCSC Ensembl
Innerchr5:29421621..29461973hg19UCSC Ensembl
Outerchr5:29421621..29461973hg19UCSC Ensembl
Innerchr5:29457378..29497730hg18UCSC Ensembl
Outerchr5:29457378..29497730hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3840353
hg1940353
hg1840353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785708
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894165
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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