A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894006



Internal ID19184860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:113384028..113411549hg38UCSC Ensembl
Outerchr4:113384028..113411549hg38UCSC Ensembl
Innerchr4:114305184..114332705hg19UCSC Ensembl
Outerchr4:114305184..114332705hg19UCSC Ensembl
Innerchr4:114524633..114552154hg18UCSC Ensembl
Outerchr4:114524633..114552154hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3827522
hg1927522
hg1827522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785989
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894006
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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