A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668757



Internal ID9934862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90998823..91003674hg38UCSC Ensembl
chr9:93761105..93765956hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg384852
hg194852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5856740, essv5857087, essv5643052, essv5669789, essv6110853
SamplesNA19457, NA19313, NA19372, NA19338, NA19334
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668757
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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