A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998803



Internal ID7064556
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586478
SamplesHuRef
Known GenesSULT1A1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998803
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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