A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892910



Internal ID19183730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80879772..80903648hg38UCSC Ensembl
Outerchr16:80870512..80903648hg38UCSC Ensembl
Innerchr16:80913669..80937545hg19UCSC Ensembl
Outerchr16:80904409..80937545hg19UCSC Ensembl
Innerchr16:79471170..79495046hg18UCSC Ensembl
Outerchr16:79461910..79495046hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3833137
hg1933137
hg1833137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780495, essv25779250
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892910
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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