A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015928



Internal ID18758462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33386069..33468684hg38UCSC Ensembl
Innerchr9:33386067..33468682hg19UCSC Ensembl
Innerchr9:33376067..33458682hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3882616
hg1982616
hg1882616
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7517n100
Supporting Variantsnssv3688877
Samples
Known GenesAQP3, AQP7, MIR6851, NOL6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015928
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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