A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676670



Internal ID9942775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107473233..107476141hg38UCSC Ensembl
chr9:110235514..110238422hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382909
hg192909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5496394
SamplesNA18619
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676670
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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