A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7349n100



Internal ID22793436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:162695..297866hg38UCSC Ensembl
chr9:162695..297866hg19UCSC Ensembl
chr9:152695..287866hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38135172
hg19135172
hg18135172
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019733, nsv1022969, nsv1031437, nsv1016390, nsv1018435
Samples
Known GenesC9orf66, CBWD1, DOCK8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7349n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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