A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7475n100



Internal ID19017843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21455761..21525000hg38UCSC Ensembl
chr9:21455760..21524999hg19UCSC Ensembl
chr9:21445760..21514999hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3869240
hg1969240
hg1869240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020445, nsv1020232, nsv1030064
Samples
Known GenesIFNE, MIR31, MIR31HG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7475n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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