A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3445711



Internal ID15292662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65758915..65762413hg38UCSC Ensembl
Innerchr9:65759915..65761413hg38UCSC Ensembl
Outerchr9:65757915..65763413hg38UCSC Ensembl
chr9:70403632..70407130hg19UCSC Ensembl
Innerchr9:70404632..70406130hg19UCSC Ensembl
Outerchr9:70402632..70408130hg19UCSC Ensembl
chr9:69643452..69646950hg18UCSC Ensembl
Innerchr9:69644452..69645950hg18UCSC Ensembl
Outerchr9:69642452..69647950hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg383499
hg193499
hg183499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4427e59
Supporting Variantsessv8697317
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3445711
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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