A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669427



Internal ID9935532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76535034..76545828hg38UCSC Ensembl
Outerchr9:76534877..76545983hg38UCSC Ensembl
Innerchr9:79149950..79160744hg19UCSC Ensembl
Outerchr9:79149793..79160899hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3811107
hg1911107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6245043, essv5832923
SamplesHG00125, HG00123
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669427
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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