A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5921125



Internal ID8898528
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 Flag1
Merged StatusS
Merged Variantsesv2661147
Supporting Variants
SamplesHG01073
Known GenesRBM23
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5921125
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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