A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7476n100



Internal ID22793563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22740233..22795972hg38UCSC Ensembl
chr9:22740232..22795971hg19UCSC Ensembl
chr9:22730232..22785971hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3855740
hg1955740
hg1855740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026544, nsv1030847
Samples
Known GenesFLJ35282
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7476n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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