A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3286n100



Internal ID22789373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79162909..79236145hg38UCSC Ensembl
chr17:77158991..77232227hg19UCSC Ensembl
chr17:74670586..74743822hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3873237
hg1973237
hg1873237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063443, nsv1058429
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)dgv3286n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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