A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892879



Internal ID18837013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69998055..70102302hg38UCSC Ensembl
Outerchr16:69990399..70157430hg38UCSC Ensembl
Innerchr16:70031958..70136205hg19UCSC Ensembl
Outerchr16:70024302..70191333hg19UCSC Ensembl
Innerchr16:68589459..68693706hg18UCSC Ensembl
Outerchr16:68581803..68748834hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38167032
hg19167032
hg18167032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790220, essv25792757, essv25789005, essv25789469
Samples
Known GenesMIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892879
Frequency
Sample Size3017
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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