A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021015



Internal ID19110233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..370439hg38UCSC Ensembl
Innerchr9:46587..370439hg19UCSC Ensembl
Innerchr9:36587..360439hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38323853
hg19323853
hg18323853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7345n100
Supporting Variantsnssv3690952
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)nsv1021015
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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