A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658053



Internal ID9577472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36373668..36376705hg38UCSC Ensembl
Outerchr18:36373511..36376858hg38UCSC Ensembl
Innerchr18:33953631..33956668hg19UCSC Ensembl
Outerchr18:33953474..33956821hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg383348
hg193348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6030129
SamplesNA18510
Known GenesFHOD3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658053
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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