A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662592



Internal ID9928697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:26750372..26760936hg38UCSC Ensembl
Outerchr18:26750215..26761089hg38UCSC Ensembl
Innerchr18:24330336..24340900hg19UCSC Ensembl
Outerchr18:24330179..24341053hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3810875
hg1910875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6127240, essv6595330
SamplesHG00702, HG00656
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662592
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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