A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660826



Internal ID9926931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:34233831..34235235hg38UCSC Ensembl
Outerchr18:34233794..34235285hg38UCSC Ensembl
Innerchr18:31813795..31815199hg19UCSC Ensembl
Outerchr18:31813758..31815249hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381492
hg191492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6054842
SamplesNA18870
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660826
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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