A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671754



Internal ID9937859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52083596..52086149hg38UCSC Ensembl
chr15:52375793..52378346hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg382554
hg192554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6474427, essv5739289
SamplesNA19066, NA18980
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671754
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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