A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3383969



Internal ID15230939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46579873..46584971hg38UCSC Ensembl
Innerchr10:46580873..46583971hg38UCSC Ensembl
Outerchr10:46578873..46585971hg38UCSC Ensembl
chr10:46964646..46969744hg19UCSC Ensembl
Innerchr10:46965646..46968744hg19UCSC Ensembl
Outerchr10:46963646..46970744hg19UCSC Ensembl
chr10:46384652..46389750hg18UCSC Ensembl
Innerchr10:46385652..46388750hg18UCSC Ensembl
Outerchr10:46383652..46390750hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg385099
hg195099
hg185099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv410e59
Supporting Variantsessv8688066
SamplesNA12892
Known GenesSYT15
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3383969
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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