A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788299



Internal ID18825595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133443258..133536297hg38UCSC Ensembl
Innerchr10:135256762..135349801hg19UCSC Ensembl
Innerchr10:135106752..135199791hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3893040
hg1993040
hg1893040
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891902
Supporting Variants
Samples
Known GenesCYP2E1, SCART1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=49
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788299
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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