A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664092



Internal ID9930197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129234158..129245161hg38UCSC Ensembl
Outerchr9:129234001..129245314hg38UCSC Ensembl
Innerchr9:131996437..132007440hg19UCSC Ensembl
Outerchr9:131996280..132007593hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3811314
hg1911314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6383583
SamplesNA18632
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664092
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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