A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893771



Internal ID19184591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:121624653..121634407hg38UCSC Ensembl
Outerchr3:121624653..121634407hg38UCSC Ensembl
Innerchr3:121343500..121353254hg19UCSC Ensembl
Outerchr3:121343500..121353254hg19UCSC Ensembl
Innerchr3:122826190..122835944hg18UCSC Ensembl
Outerchr3:122826190..122835944hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg389755
hg199755
hg189755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782737
Samples
Known GenesFBXO40, HCLS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893771
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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