A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659569



Internal ID9578988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:55531046..55535112hg38UCSC Ensembl
Outerchr18:55531009..55535162hg38UCSC Ensembl
Innerchr18:53198277..53202343hg19UCSC Ensembl
Outerchr18:53198240..53202393hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg384154
hg194154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5817019
SamplesHG00595
Known GenesTCF4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659569
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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