A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891886



Internal ID18839596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94694399..94965778hg38UCSC Ensembl
Outerchr10:94694399..94965778hg38UCSC Ensembl
Innerchr10:96454156..96725535hg19UCSC Ensembl
Outerchr10:96454156..96725535hg19UCSC Ensembl
Innerchr10:96444146..96715525hg18UCSC Ensembl
Outerchr10:96444146..96715525hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38271380
hg19271380
hg18271380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787734
Samples
Known GenesCYP2C18, CYP2C19, CYP2C9
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891886
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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