A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994369



Internal ID6730324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7196037..7196571hg38UCSC Ensembl
Innerchr16:7246038..7246572hg19UCSC Ensembl
Innerchr16:7186039..7186573hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38535
hg19535
hg18535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586951
SamplesHuRef
Known GenesRBFOX1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994369
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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