A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026546



Internal ID19115764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..290670hg38UCSC Ensembl
Innerchr9:46587..290670hg19UCSC Ensembl
Innerchr9:36587..280670hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38244084
hg19244084
hg18244084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7344n100
Supporting Variantsnssv3690946, nssv3690945
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)nsv1026546
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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