A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894032



Internal ID19184886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130892744..131038446hg38UCSC Ensembl
Outerchr4:130892744..131038446hg38UCSC Ensembl
Innerchr4:131813899..131959601hg19UCSC Ensembl
Outerchr4:131813899..131959601hg19UCSC Ensembl
Innerchr4:132033349..132179051hg18UCSC Ensembl
Outerchr4:132033349..132179051hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38145703
hg19145703
hg18145703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790682
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894032
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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