A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3376182



Internal ID15223155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65740815..65758413hg38UCSC Ensembl
Innerchr9:65741815..65757413hg38UCSC Ensembl
Outerchr9:65739815..65759413hg38UCSC Ensembl
chr9:70407632..70425230hg19UCSC Ensembl
Innerchr9:70408632..70424230hg19UCSC Ensembl
Outerchr9:70406632..70426230hg19UCSC Ensembl
chr9:69647452..69665050hg18UCSC Ensembl
Innerchr9:69648452..69664050hg18UCSC Ensembl
Outerchr9:69646452..69666050hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3817599
hg1917599
hg1817599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4428e59
Supporting Variantsessv8697323
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3376182
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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