A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665372



Internal ID9931477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76201410..76210682hg38UCSC Ensembl
Outerchr18:76201373..76210732hg38UCSC Ensembl
Innerchr18:73913365..73922637hg19UCSC Ensembl
Outerchr18:73913328..73922687hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg389360
hg199360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6335625
SamplesHG00698
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665372
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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