A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7347n100



Internal ID22793434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88018..358384hg38UCSC Ensembl
chr9:88018..358384hg19UCSC Ensembl
chr9:78018..348384hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38270367
hg19270367
hg18270367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033689, nsv1015260
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7347n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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