A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658701



Internal ID9924806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62490974..62492229hg38UCSC Ensembl
chr18:60158207..60159462hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg381256
hg191256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6592958
SamplesNA19360
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658701
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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