A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893915



Internal ID19184769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34829521..35017558hg38UCSC Ensembl
Outerchr4:34829521..35017558hg38UCSC Ensembl
Innerchr4:34831143..35019180hg19UCSC Ensembl
Outerchr4:34831143..35019180hg19UCSC Ensembl
Innerchr4:34507538..34695575hg18UCSC Ensembl
Outerchr4:34507538..34695575hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38188038
hg19188038
hg18188038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783813
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893915
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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