A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659715



Internal ID9925820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34266800..34282483hg38UCSC Ensembl
Outerchr9:34266763..34282533hg38UCSC Ensembl
Innerchr9:34266798..34282481hg19UCSC Ensembl
Outerchr9:34266761..34282531hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3815771
hg1915771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6435590
SamplesNA18602
Known GenesKIF24
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659715
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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