A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892773



Internal ID18836907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7012444..7019055hg38UCSC Ensembl
Outerchr16:7012444..7019055hg38UCSC Ensembl
Innerchr16:7062445..7069056hg19UCSC Ensembl
Outerchr16:7062445..7069056hg19UCSC Ensembl
Innerchr16:7002446..7009057hg18UCSC Ensembl
Outerchr16:7002446..7009057hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg386612
hg196612
hg186612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799188, essv25798855, essv25797404, essv25800606, essv25794260, essv25783223, essv25798677, essv25798503
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892773
Frequency
Sample Size3017
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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