A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587120



Internal ID7058502
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv993722
Supporting Variants
SamplesHuRef
Known GenesSULT1A1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587120
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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