A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3411153



Internal ID15258113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63292060..63301958hg38UCSC Ensembl
Innerchr9:63293060..63300958hg38UCSC Ensembl
Outerchr9:63291060..63302958hg38UCSC Ensembl
chr9:67247032..67256930hg19UCSC Ensembl
Innerchr9:67248032..67255930hg19UCSC Ensembl
Outerchr9:67246032..67257930hg19UCSC Ensembl
chr9:66936852..66946750hg18UCSC Ensembl
Innerchr9:66937852..66945750hg18UCSC Ensembl
Outerchr9:66935852..66947750hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg389899
hg199899
hg189899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697110
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3411153
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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