A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659552



Internal ID9925657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122540811..122598369hg38UCSC Ensembl
chr9:125303090..125360648hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3857559
hg1957559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5485586, essv5707637, essv6222611, essv6076452
SamplesHG00334, HG00264, HG00275, NA19440
Known GenesOR1L8, OR1N2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659552
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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