A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7346n100



Internal ID22793433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:46587..518103hg38UCSC Ensembl
chr9:46587..518103hg19UCSC Ensembl
chr9:36587..508103hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38471517
hg19471517
hg18471517
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021131, nsv1018439, nsv1029333, nsv1033067, nsv1024015
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4, KANK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7346n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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