A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790276



Internal ID18813037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7044206..7155296hg38UCSC Ensembl
Innerchr16:7094207..7205297hg19UCSC Ensembl
Innerchr16:7034208..7145298hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38111091
hg19111091
hg18111091
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892779
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=69
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790276
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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