A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660776



Internal ID9926881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22276800..22290708hg38UCSC Ensembl
chr10:22565729..22579637hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3813909
hg1913909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6186675
SamplesHG00640
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660776
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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