A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676526



Internal ID9942631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36778971..36785481hg38UCSC Ensembl
Innerchr21:38151272..38157782hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg386511
hg196511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5443149, essv5663145
SamplesNA19238, NA19240
Known GenesHLCS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676526
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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