A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892779



Internal ID18836913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7044206..7155296hg38UCSC Ensembl
Outerchr16:7044206..7155296hg38UCSC Ensembl
Innerchr16:7094207..7205297hg19UCSC Ensembl
Outerchr16:7094207..7205297hg19UCSC Ensembl
Innerchr16:7034208..7145298hg18UCSC Ensembl
Outerchr16:7034208..7145298hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38111091
hg19111091
hg18111091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790276
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892779
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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