A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661829



Internal ID9927934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65772085..65872188hg38UCSC Ensembl
chr10:67531843..67631946hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38100104
hg19100104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5525947
SamplesNA19469
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661829
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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