A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671036



Internal ID9937141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92214363..92227983hg38UCSC Ensembl
chr10:93974120..93987740hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3813621
hg1913621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5676389
SamplesHG01149
Known GenesCPEB3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671036
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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