A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893920



Internal ID19184774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43531651..43984517hg38UCSC Ensembl
Outerchr4:43531651..43984517hg38UCSC Ensembl
Innerchr4:43533668..43986534hg19UCSC Ensembl
Outerchr4:43533668..43986534hg19UCSC Ensembl
Innerchr4:43228425..43681291hg18UCSC Ensembl
Outerchr4:43228425..43681291hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38452867
hg19452867
hg18452867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781453
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893920
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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