A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016390



Internal ID19105609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:162695..259224hg38UCSC Ensembl
Innerchr9:162695..259224hg19UCSC Ensembl
Innerchr9:152695..249224hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3896530
hg1996530
hg1896530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7349n100
Supporting Variantsnssv3690966
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)nsv1016390
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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