A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3399983



Internal ID15246946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63295860..63301258hg38UCSC Ensembl
Innerchr9:63296860..63300258hg38UCSC Ensembl
Outerchr9:63294860..63302258hg38UCSC Ensembl
chr9:67250832..67256230hg19UCSC Ensembl
Innerchr9:67251832..67255230hg19UCSC Ensembl
Outerchr9:67249832..67257230hg19UCSC Ensembl
chr9:66940652..66946050hg18UCSC Ensembl
Innerchr9:66941652..66945050hg18UCSC Ensembl
Outerchr9:66939652..66947050hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg385399
hg195399
hg185399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4397e59
Supporting Variantsessv8697111
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3399983
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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