A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893889



Internal ID18838023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17807915..17817512hg38UCSC Ensembl
Outerchr4:17807915..17817512hg38UCSC Ensembl
Innerchr4:17809538..17819135hg19UCSC Ensembl
Outerchr4:17809538..17819135hg19UCSC Ensembl
Innerchr4:17418636..17428233hg18UCSC Ensembl
Outerchr4:17418636..17428233hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg389598
hg199598
hg189598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787319
Samples
Known GenesDCAF16, NCAPG
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893889
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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