A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12447n54



Internal ID20145871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39037..358932hg38UCSC Ensembl
chr9:39037..358932hg19UCSC Ensembl
chr9:29037..348932hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38319896
hg19319896
hg18319896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv612981, nsv612985, nsv612984
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12447n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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