A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894080



Internal ID19184934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:178306444..178470479hg38UCSC Ensembl
Outerchr4:178306444..178470479hg38UCSC Ensembl
Innerchr4:179227598..179391633hg19UCSC Ensembl
Outerchr4:179227598..179391633hg19UCSC Ensembl
Innerchr4:179464592..179628627hg18UCSC Ensembl
Outerchr4:179464592..179628627hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38164036
hg19164036
hg18164036
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792520
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894080
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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