A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893972



Internal ID19184826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:83170291..83202545hg38UCSC Ensembl
Outerchr4:83170291..83202545hg38UCSC Ensembl
Innerchr4:84091444..84123698hg19UCSC Ensembl
Outerchr4:84091444..84123698hg19UCSC Ensembl
Innerchr4:84310468..84342722hg18UCSC Ensembl
Outerchr4:84310468..84342722hg18UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3832255
hg1932255
hg1832255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796199
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893972
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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