A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3346588



Internal ID15193570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41185103..41192001hg38UCSC Ensembl
Innerchr9:41186103..41191001hg38UCSC Ensembl
Outerchr9:41184103..41193001hg38UCSC Ensembl
chr9:69258332..69265230hg19UCSC Ensembl
Innerchr9:69259332..69264230hg19UCSC Ensembl
Outerchr9:69257332..69266230hg19UCSC Ensembl
chr9:68548152..68555050hg18UCSC Ensembl
Innerchr9:68549152..68554050hg18UCSC Ensembl
Outerchr9:68547152..68556050hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg386899
hg196899
hg186899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697196
SamplesNA12878
Known GenesCBWD5, CBWD6
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3346588
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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