A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663826



Internal ID9583245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96136332..96140928hg38UCSC Ensembl
Outerchr13:96136295..96140978hg38UCSC Ensembl
Innerchr13:96788586..96793182hg19UCSC Ensembl
Outerchr13:96788549..96793232hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg384684
hg194684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5446564
SamplesNA20778
Known GenesHS6ST3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663826
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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