A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659839



Internal ID9579258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32068027..32070114hg38UCSC Ensembl
chr2:32293096..32295183hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg382088
hg192088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5594117
SamplesNA19700
Known GenesSPAST
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659839
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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