A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672550



Internal ID9938655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35057812..35060655hg38UCSC Ensembl
chr21:36430109..36432952hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg382844
hg192844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6397299
SamplesNA19390
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672550
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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