A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019676



Internal ID19108894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:525752..804603hg38UCSC Ensembl
Innerchr9:525752..804603hg19UCSC Ensembl
Innerchr9:515752..794603hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38278852
hg19278852
hg18278852
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7363n100
Supporting Variantsnssv3691034
Samples
Known GenesKANK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019676
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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