A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675867



Internal ID9941972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43349502..43357765hg38UCSC Ensembl
chr10:43844950..43853213hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg388264
hg198264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5817509
SamplesNA20510
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675867
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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