A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1005n100



Internal ID19011373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133451264..133534223hg38UCSC Ensembl
chr10:135264768..135347727hg19UCSC Ensembl
chr10:135114758..135197717hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3882960
hg1982960
hg1882960
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036324, nsv1054621
Samples
Known GenesCYP2E1, SCART1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1005n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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