A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674387



Internal ID9940492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100503663..100504374hg38UCSC Ensembl
chr15:101043868..101044579hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6210246, essv6064085
SamplesNA19445, NA19453
Known GenesCERS3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674387
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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