A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892777



Internal ID18836911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6943054..6951230hg38UCSC Ensembl
Outerchr16:6943054..6951230hg38UCSC Ensembl
Innerchr16:6993055..7001231hg19UCSC Ensembl
Outerchr16:6993055..7001231hg19UCSC Ensembl
Innerchr16:6933056..6941232hg18UCSC Ensembl
Outerchr16:6933056..6941232hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg388177
hg198177
hg188177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796164
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892777
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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