A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892867



Internal ID19183687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:59472207..59658722hg38UCSC Ensembl
Outerchr16:59472207..59658722hg38UCSC Ensembl
Innerchr16:59506111..59692626hg19UCSC Ensembl
Outerchr16:59506111..59692626hg19UCSC Ensembl
Innerchr16:58063612..58250127hg18UCSC Ensembl
Outerchr16:58063612..58250127hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38186516
hg19186516
hg18186516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778267
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892867
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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