A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894161



Internal ID19185230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28763545..28824481hg38UCSC Ensembl
Outerchr5:28763545..28824481hg38UCSC Ensembl
Innerchr5:28763652..28824588hg19UCSC Ensembl
Outerchr5:28763652..28824588hg19UCSC Ensembl
Innerchr5:28799409..28860345hg18UCSC Ensembl
Outerchr5:28799409..28860345hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3860937
hg1960937
hg1860937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780057
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894161
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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