A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3207123



Internal ID10880103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:6907738..6908440hg38UCSC Ensembl
Outerchr16:6957739..6958441hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7476690
SamplesHuRef
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3207123
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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