A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666599



Internal ID9932704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122185499..122186668hg38UCSC Ensembl
Outerchr10:122185342..122186821hg38UCSC Ensembl
Innerchr10:123945014..123946183hg19UCSC Ensembl
Outerchr10:123944857..123946336hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381480
hg191480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5953570, essv6382435, essv6469191
SamplesNA19076, NA18559, NA18623
Known GenesTACC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666599
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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