A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663668



Internal ID9929773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71009367..71013229hg38UCSC Ensembl
chr17:69005508..69009370hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg383863
hg193863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5828329
SamplesHG00500
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663668
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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