A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662680



Internal ID9582099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:76010663..76013200hg38UCSC Ensembl
Outerchr4:76010506..76013353hg38UCSC Ensembl
Innerchr4:76931816..76934353hg19UCSC Ensembl
Outerchr4:76931659..76934506hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg382848
hg192848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6116556
SamplesNA18982
Known GenesART3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662680
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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