A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892768



Internal ID18836902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6041894..6068537hg38UCSC Ensembl
Outerchr16:6041894..6068537hg38UCSC Ensembl
Innerchr16:6091895..6118538hg19UCSC Ensembl
Outerchr16:6091895..6118538hg19UCSC Ensembl
Innerchr16:6031896..6058539hg18UCSC Ensembl
Outerchr16:6031896..6058539hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3826644
hg1926644
hg1826644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796276
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892768
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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