A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660100



Internal ID9579519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39723462..39731242hg38UCSC Ensembl
chr21:41095389..41103169hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg387781
hg197781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5561639
SamplesNA19060
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660100
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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