A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893952



Internal ID18838120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68955731..69264211hg38UCSC Ensembl
Outerchr4:68955731..69264211hg38UCSC Ensembl
Innerchr4:69821449..70129929hg19UCSC Ensembl
Outerchr4:69821449..70129929hg19UCSC Ensembl
Innerchr4:69856038..70164518hg18UCSC Ensembl
Outerchr4:69856038..70164518hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38308481
hg19308481
hg18308481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778726
Samples
Known GenesUGT2B10, UGT2B11, UGT2B7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893952
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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