A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663999



Internal ID9930104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80809359..80815123hg38UCSC Ensembl
Outerchr10:80809322..80815173hg38UCSC Ensembl
Innerchr10:82569115..82574879hg19UCSC Ensembl
Outerchr10:82569078..82574929hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg385852
hg195852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5578032
SamplesHG00560
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663999
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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