A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678432



Internal ID9944537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96054197..96056669hg38UCSC Ensembl
chr15:96597426..96599898hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg382473
hg192473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5482126
SamplesNA19462
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678432
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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