A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659260



Internal ID9578679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93064404..93065552hg38UCSC Ensembl
Outerchr9:93064367..93065602hg38UCSC Ensembl
Innerchr9:95826686..95827834hg19UCSC Ensembl
Outerchr9:95826649..95827884hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381236
hg191236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5910822
SamplesNA19056
Known GenesSUSD3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659260
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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