A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668079



Internal ID9934184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:26943392..26954841hg38UCSC Ensembl
Outerchr18:26943355..26954891hg38UCSC Ensembl
Innerchr18:24523356..24534805hg19UCSC Ensembl
Outerchr18:24523319..24534855hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3811537
hg1911537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6484342
SamplesHG00278
Known GenesCHST9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668079
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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