A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659158



Internal ID9925263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:40098499..40103924hg38UCSC Ensembl
Outerchr20:40098462..40103974hg38UCSC Ensembl
Innerchr20:38727140..38732565hg19UCSC Ensembl
Outerchr20:38727103..38732615hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg385513
hg195513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5961445, essv6171995
SamplesHG00143, HG00123
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659158
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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