A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659058



Internal ID9925163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184236950..184247937hg38UCSC Ensembl
Outerchr4:184236793..184248090hg38UCSC Ensembl
Innerchr4:185158103..185169090hg19UCSC Ensembl
Outerchr4:185157946..185169243hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3811298
hg1911298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6121628
SamplesNA10851
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659058
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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