A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7472n100



Internal ID22793559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20264854..20287646hg38UCSC Ensembl
chr9:20264852..20287644hg19UCSC Ensembl
chr9:20254852..20277644hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3822793
hg1922793
hg1822793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025955, nsv1032703, nsv1016273
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7472n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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