A curated catalogue of human genomic structural variation




Variant Details

Variant: esv993722



Internal ID7062634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28606050..28606822hg38UCSC Ensembl
Innerchr16:28617371..28618143hg19UCSC Ensembl
Innerchr16:28524872..28525644hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38773
hg19773
hg18773
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587120
SamplesHuRef
Known GenesSULT1A1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv993722
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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