A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5891705



Internal ID8869108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38976480..38978127hg38UCSC Ensembl
Outerchr21:38976443..38978177hg38UCSC Ensembl
Innerchr21:40348406..40350053hg19UCSC Ensembl
Outerchr21:40348369..40350103hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg381735
hg191735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677138
Supporting Variants
SamplesNA19474
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5891705
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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