A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587036



Internal ID6711732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6842071..6843522hg38UCSC Ensembl
Innerchr16:6892072..6893523hg19UCSC Ensembl
Innerchr16:6832073..6833524hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381452
hg191452
hg181452
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1002783
Supporting Variants
SamplesHuRef
Known GenesRBFOX1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587036
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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