A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656952



Internal ID9923057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13951865..13955586hg38UCSC Ensembl
chr4:13953489..13957210hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg383722
hg193722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5919625
SamplesNA18950
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656952
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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