A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893862



Internal ID18837996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148766..427832hg38UCSC Ensembl
Outerchr4:148766..427832hg38UCSC Ensembl
Innerchr4:142550..421621hg19UCSC Ensembl
Outerchr4:142550..421621hg19UCSC Ensembl
Innerchr4:132550..411621hg18UCSC Ensembl
Outerchr4:132550..411621hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38279067
hg19279072
hg18279072
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790839
Samples
Known GenesABCA11P, ZNF141, ZNF718, ZNF732, ZNF876P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893862
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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