A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664298



Internal ID9583717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:75136222..75149532hg38UCSC Ensembl
Outerchr2:75136185..75149582hg38UCSC Ensembl
Innerchr2:75363348..75376658hg19UCSC Ensembl
Outerchr2:75363311..75376708hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3813398
hg1913398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5541569
SamplesNA12154
Known GenesTACR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664298
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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