A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658645



Internal ID9924750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104717831..104729133hg38UCSC Ensembl
chr9:107480112..107491414hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3811303
hg1911303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6034929, essv5870760, essv5408480, essv5756120, essv6329043, essv5461950
SamplesNA12273, HG00151, NA12283, HG00152, HG00265, HG00375
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658645
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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