A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509827



Internal ID18461422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133400840..133600187hg38UCSC Ensembl
Innerchr10:135214344..135413691hg19UCSC Ensembl
Innerchr10:135064334..135263681hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38199348
hg19199348
hg18199348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043323
Supporting Variants
Samples
Known GenesCYP2E1, MTG1, SCART1, SPRN, SPRNP1, SYCE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509827
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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