A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668911



Internal ID9935016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43336042..43336391hg38UCSC Ensembl
Outerchr21:43336005..43336441hg38UCSC Ensembl
Innerchr21:44755922..44756271hg19UCSC Ensembl
Outerchr21:44755885..44756321hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6444924, essv6223426, essv6592223, essv6277973, essv6263149, essv6446487, essv5600672, essv6539230
SamplesNA20507, HG00281, HG01495, NA19371, NA18934, NA18516, NA19452, NA19093
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668911
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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