A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658819



Internal ID9924924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58043835..58052956hg38UCSC Ensembl
chr15:58336033..58345154hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg389122
hg199122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5802576
SamplesNA11843
Known GenesALDH1A2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658819
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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