A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665893



Internal ID9585312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60966432..60968231hg38UCSC Ensembl
Outerchr17:60966394..60968281hg38UCSC Ensembl
Innerchr17:59043793..59045592hg19UCSC Ensembl
Outerchr17:59043755..59045642hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381888
hg191888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5565470
SamplesNA18986
Known GenesBCAS3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665893
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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