A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675157



Internal ID9941262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22317626..22318509hg38UCSC Ensembl
Outerchr18:22317589..22318559hg38UCSC Ensembl
Innerchr18:19897589..19898472hg19UCSC Ensembl
Outerchr18:19897552..19898522hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38971
hg19971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5929402
SamplesHG00663
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675157
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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