A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894202



Internal ID19185271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:63152122..63233859hg38UCSC Ensembl
Outerchr5:63152122..63233859hg38UCSC Ensembl
Innerchr5:62447949..62529686hg19UCSC Ensembl
Outerchr5:62447949..62529686hg19UCSC Ensembl
Innerchr5:62483705..62565442hg18UCSC Ensembl
Outerchr5:62483705..62565442hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3881738
hg1981738
hg1881738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779745
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894202
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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