A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667631



Internal ID9587050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16988100..17064854hg38UCSC Ensembl
Outerchr9:16988063..17064904hg38UCSC Ensembl
Innerchr9:16988098..17064852hg19UCSC Ensembl
Outerchr9:16988061..17064902hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3876842
hg1976842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6435593
SamplesNA20756
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667631
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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