A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676771



Internal ID9942876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:153838181..153840063hg38UCSC Ensembl
Outerchr4:153838144..153840113hg38UCSC Ensembl
Innerchr4:154759333..154761215hg19UCSC Ensembl
Outerchr4:154759296..154761265hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg381970
hg191970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5422574
SamplesNA20828
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676771
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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