A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3442658



Internal ID14942925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65659644..65675313hg38UCSC Ensembl
Innerchr9:65660645..65674313hg38UCSC Ensembl
Outerchr9:65659539..65676313hg38UCSC Ensembl
chr9:70490732..70506430hg19UCSC Ensembl
Innerchr9:70491732..70505430hg19UCSC Ensembl
Outerchr9:70489732..70506535hg19UCSC Ensembl
chr9:69730552..69746250hg18UCSC Ensembl
Innerchr9:69731552..69745250hg18UCSC Ensembl
Outerchr9:69729552..69747250hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3815670
hg1915699
hg1815699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4429e59
Supporting Variantsessv8697328
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3442658
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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