A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3290n100



Internal ID22789377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79363311..79471877hg38UCSC Ensembl
chr17:77359393..77467959hg19UCSC Ensembl
chr17:74870988..74979554hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38108567
hg19108567
hg18108567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056051, nsv1063129
Samples
Known GenesRBFOX3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3290n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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