A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662895



Internal ID9929000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:63473375..63521938hg38UCSC Ensembl
Outerchr4:63473338..63521988hg38UCSC Ensembl
Innerchr4:64339093..64387656hg19UCSC Ensembl
Outerchr4:64339056..64387706hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3848651
hg1948651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6520602
SamplesNA20588
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662895
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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