A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891903



Internal ID18839613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133534223..133572278hg38UCSC Ensembl
Outerchr10:133534223..133572278hg38UCSC Ensembl
Innerchr10:135347727..135385782hg19UCSC Ensembl
Outerchr10:135347727..135385782hg19UCSC Ensembl
Innerchr10:135197717..135235772hg18UCSC Ensembl
Outerchr10:135197717..135235772hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3838056
hg1938056
hg1838056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792167
Samples
Known GenesCYP2E1, SPRNP1, SYCE1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891903
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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