A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690683



Internal ID18642278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19288977..19399899hg38UCSC Ensembl
Innerchr9:19288975..19399897hg19UCSC Ensembl
Innerchr9:19278975..19389897hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38110923
hg19110923
hg18110923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030736
Supporting Variants
Samples
Known GenesDENND4C, RPS6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690683
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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