A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661658



Internal ID9927763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118658588..118661358hg38UCSC Ensembl
chr9:121420866..121423636hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382771
hg192771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5764477, essv6257854, essv6324268, essv6117815, essv6157073
SamplesNA11918, HG00334, HG01183, HG00329, HG00180
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661658
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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