A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667255



Internal ID9586674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89846945..89851628hg38UCSC Ensembl
chr15:90390177..90394860hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384684
hg194684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6232215
SamplesNA18977
Known GenesAP3S2, C15orf38-AP3S2, MIR5094
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667255
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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