A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3287n100



Internal ID22789374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79190963..79238589hg38UCSC Ensembl
chr17:77187045..77234671hg19UCSC Ensembl
chr17:74698640..74746266hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3847627
hg1947627
hg1847627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058147, nsv1058055, nsv1066228
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)dgv3287n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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