A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666984



Internal ID9933089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:29030043..29033421hg38UCSC Ensembl
Outerchr17:29029884..29033593hg38UCSC Ensembl
Innerchr17:27357061..27360439hg19UCSC Ensembl
Outerchr17:27356902..27360611hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383710
hg193710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5405085
SamplesNA18613
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666984
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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