A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510969



Internal ID18462564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133438600..133560087hg38UCSC Ensembl
Innerchr10:135252104..135373591hg19UCSC Ensembl
Innerchr10:135102094..135223581hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38121488
hg19121488
hg18121488
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048782
Supporting Variants
Samples
Known GenesCYP2E1, SCART1, SYCE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3510969
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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