A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1006n100



Internal ID19011374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133451264..133573736hg38UCSC Ensembl
chr10:135264768..135387240hg19UCSC Ensembl
chr10:135114758..135237230hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38122473
hg19122473
hg18122473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049790, nsv1052049
Samples
Known GenesCYP2E1, SCART1, 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)dgv1006n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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