A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661364



Internal ID9927469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:60846823..60855384hg38UCSC Ensembl
Outerchr2:60846666..60855537hg38UCSC Ensembl
Innerchr2:61073958..61082519hg19UCSC Ensembl
Outerchr2:61073801..61082672hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg388872
hg198872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5882419
SamplesNA19334
Known GenesFLJ16341
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661364
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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