A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3369689



Internal ID15216665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63037860..63042958hg38UCSC Ensembl
Innerchr9:63038860..63041958hg38UCSC Ensembl
Outerchr9:63036860..63043958hg38UCSC Ensembl
chr9:66942832..66947930hg19UCSC Ensembl
Innerchr9:66943832..66946930hg19UCSC Ensembl
Outerchr9:66941832..66948930hg19UCSC Ensembl
chr9:66682652..66687750hg18UCSC Ensembl
Innerchr9:66683652..66686750hg18UCSC Ensembl
Outerchr9:66681652..66688750hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg385099
hg195099
hg185099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697083
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3369689
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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