A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660408



Internal ID9926513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37247250..37252032hg38UCSC Ensembl
Outerchr22:37247093..37252185hg38UCSC Ensembl
Innerchr22:37643290..37648072hg19UCSC Ensembl
Outerchr22:37643133..37648225hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385093
hg195093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5521657, essv6563313
SamplesHG00327, HG00274
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660408
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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