A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586478



Internal ID7057860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28606224..28606755hg38UCSC Ensembl
Innerchr16:28617545..28618076hg19UCSC Ensembl
Innerchr16:28525046..28525577hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38532
hg19532
hg18532
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998803
Supporting Variants
SamplesHuRef
Known GenesSULT1A1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586478
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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