A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893911



Internal ID19184765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:32709886..34778015hg38UCSC Ensembl
Outerchr4:32709886..34778015hg38UCSC Ensembl
Innerchr4:32711508..34779637hg19UCSC Ensembl
Outerchr4:32711508..34779637hg19UCSC Ensembl
Innerchr4:32355406..34456032hg18UCSC Ensembl
Outerchr4:32355406..34456032hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg382068130
hg192068130
hg182100627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783812
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893911
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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