A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667936



Internal ID9934041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67800015..67804531hg38UCSC Ensembl
Outerchr17:67799978..67804581hg38UCSC Ensembl
Innerchr17:65796131..65800647hg19UCSC Ensembl
Outerchr17:65796094..65800697hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg384604
hg194604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5417221
SamplesNA19916
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667936
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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