A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023129



Internal ID19112346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33967101..34118050hg38UCSC Ensembl
Innerchr9:33967099..34118048hg19UCSC Ensembl
Innerchr9:33957099..34108048hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38150950
hg19150950
hg18150950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688880
Samples
Known GenesDCAF12, UBAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023129
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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