A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657584



Internal ID9923689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89493597..89496053hg38UCSC Ensembl
chr9:92108512..92110968hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382457
hg192457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6203574
SamplesNA20582
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657584
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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