A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667240



Internal ID9586659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112530545..112531627hg38UCSC Ensembl
Outerchr9:112530508..112531677hg38UCSC Ensembl
Innerchr9:115292825..115293907hg19UCSC Ensembl
Outerchr9:115292788..115293957hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381170
hg191170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5608100
SamplesNA19682
Known GenesKIAA1958
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667240
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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