A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893950



Internal ID19184804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:69188963..69305562hg38UCSC Ensembl
Outerchr4:69188963..69357164hg38UCSC Ensembl
Innerchr4:70054681..70171280hg19UCSC Ensembl
Outerchr4:70054681..70222882hg19UCSC Ensembl
Innerchr4:70089270..70205869hg18UCSC Ensembl
Outerchr4:70089270..70257471hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38168202
hg19168202
hg18168202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789421, essv25791509
Samples
Known GenesUGT2B11, UGT2B28
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893950
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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