A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894013



Internal ID19184867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:117394404..117421060hg38UCSC Ensembl
Outerchr4:117394404..117421060hg38UCSC Ensembl
Innerchr4:118315560..118342216hg19UCSC Ensembl
Outerchr4:118315560..118342216hg19UCSC Ensembl
Innerchr4:118535008..118561664hg18UCSC Ensembl
Outerchr4:118535008..118561664hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3826657
hg1926657
hg1826657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788578
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894013
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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