A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663123



Internal ID9929228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31147404..31148045hg38UCSC Ensembl
Outerchr9:31147367..31148095hg38UCSC Ensembl
Innerchr9:31147402..31148043hg19UCSC Ensembl
Outerchr9:31147365..31148093hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5750763
SamplesNA18557
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663123
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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