A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668459



Internal ID9934564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129432..133181hg38UCSC Ensembl
chr9:129432..133181hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg383750
hg193750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5980380, essv5713586, essv6271676, essv6308529, essv5963188, essv5780682
SamplesNA19819, NA19313, NA19403, NA19835, NA19713, NA19431
Known GenesCBWD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668459
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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