A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892769



Internal ID18836903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6231292..6406762hg38UCSC Ensembl
Outerchr16:6231292..6406762hg38UCSC Ensembl
Innerchr16:6281293..6456763hg19UCSC Ensembl
Outerchr16:6281293..6456763hg19UCSC Ensembl
Innerchr16:6221294..6396764hg18UCSC Ensembl
Outerchr16:6221294..6396764hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38175471
hg19175471
hg18175471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801185
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892769
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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