A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892863



Internal ID19183683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55808492..55817065hg38UCSC Ensembl
Outerchr16:55808492..55817065hg38UCSC Ensembl
Innerchr16:55842404..55850977hg19UCSC Ensembl
Outerchr16:55842404..55850977hg19UCSC Ensembl
Innerchr16:54399905..54408478hg18UCSC Ensembl
Outerchr16:54399905..54408478hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg388574
hg198574
hg188574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799055
Samples
Known GenesCES1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892863
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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