A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790279



Internal ID18835012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133442823..133554659hg38UCSC Ensembl
Innerchr10:135256327..135368163hg19UCSC Ensembl
Innerchr10:135106317..135218153hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38111837
hg19111837
hg18111837
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891902
Supporting Variants
Samples
Known GenesCYP2E1, SCART1, SYCE1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=60
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790279
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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