A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660744



Internal ID9580163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60986465..60987590hg38UCSC Ensembl
chr17:59063826..59064951hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381126
hg191126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5488088
SamplesHG00707
Known GenesBCAS3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660744
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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