A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892823



Internal ID18836957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28591670..28609430hg38UCSC Ensembl
Outerchr16:28591670..28609430hg38UCSC Ensembl
Innerchr16:28602991..28620751hg19UCSC Ensembl
Outerchr16:28602991..28620751hg19UCSC Ensembl
Innerchr16:28510492..28528252hg18UCSC Ensembl
Outerchr16:28510492..28528252hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3817761
hg1917761
hg1817761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787986
Samples
Known GenesCCDC101, SULT1A1, SULT1A2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892823
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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