A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659201



Internal ID9925306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36820547..36821420hg38UCSC Ensembl
chr21:38192847..38193720hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5997625
SamplesNA19376
Known GenesHLCS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659201
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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