A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515459



Internal ID18467054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51541690..52327063hg38UCSC Ensembl
Innerchr10:53301450..54086823hg19UCSC Ensembl
Innerchr10:52971456..53756829hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38785374
hg19785374
hg18785374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045692
Supporting Variants
Samples
Known GenesCSTF2T, DKK1, PRKG1, PRKG1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3515459
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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