A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666020



Internal ID9932125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68913474..68914164hg38UCSC Ensembl
Outerchr13:68913437..68914214hg38UCSC Ensembl
Innerchr13:69487606..69488296hg19UCSC Ensembl
Outerchr13:69487569..69488346hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38778
hg19778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6576651
SamplesHG01170
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666020
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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