A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660851



Internal ID9926956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43770409..43771760hg38UCSC Ensembl
chr17:41847777..41849128hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381352
hg191352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6330465, essv6116823, essv5726286, essv5789671
SamplesHG00179, HG00268, HG00312, HG00274
Known GenesDUSP3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660851
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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