A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660911



Internal ID9580330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146925926..146937764hg38UCSC Ensembl
chr5:146305489..146317327hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3811839
hg1911839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5504464, essv5811254
SamplesNA20509, NA12546
Known GenesPPP2R2B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660911
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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