A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674890



Internal ID9940995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185084439..185086353hg38UCSC Ensembl
Outerchr4:185084402..185086403hg38UCSC Ensembl
Innerchr4:186005593..186007507hg19UCSC Ensembl
Outerchr4:186005556..186007557hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5504919
SamplesNA19461
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674890
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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