A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661147



Internal ID9580566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22902628..22903472hg38UCSC Ensembl
chr14:23371837..23372681hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38845
hg19845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv385e199
Supporting Variantsessv5921125
SamplesHG01073
Known GenesRBM23
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661147
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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