A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789709



Internal ID18832558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133452885..133588696hg38UCSC Ensembl
Innerchr10:135266389..135402200hg19UCSC Ensembl
Innerchr10:135116379..135252190hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38135812
hg19135812
hg18135812
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891902
Supporting Variants
Samples
Known GenesCYP2E1, SCART1, SPRNP1, SYCE1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=66
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789709
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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