A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659458



Internal ID9925563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:55809322..55819929hg38UCSC Ensembl
Outerchr18:55809285..55819979hg38UCSC Ensembl
Innerchr18:53476553..53487160hg19UCSC Ensembl
Outerchr18:53476516..53487210hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3810695
hg1910695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5863817
SamplesNA18499
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659458
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer