A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5832923



Internal ID8736215
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 Flag1
Merged StatusS
Merged Variantsesv2669427
Supporting Variants
SamplesHG00123
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5832923
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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