A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030736



Internal ID18773267
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 StatusM
Merged Variants
Supporting Variantsnssv3690683
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)nsv1030736
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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