A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657426



Internal ID9923531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:26409648..26412727hg38UCSC Ensembl
Outerchr21:26409611..26412777hg38UCSC Ensembl
Innerchr21:27781967..27785046hg19UCSC Ensembl
Outerchr21:27781930..27785096hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg383167
hg193167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6133444
SamplesNA18537
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657426
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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