A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3329341



Internal ID14829618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46253310..46260108hg38UCSC Ensembl
Innerchr10:46254310..46259108hg38UCSC Ensembl
Outerchr10:46252310..46261108hg38UCSC Ensembl
chr10:47624546..47631344hg19UCSC Ensembl
Innerchr10:47625546..47630344hg19UCSC Ensembl
Outerchr10:47623546..47632344hg19UCSC Ensembl
chr10:47094552..47101350hg18UCSC Ensembl
Innerchr10:47095552..47100350hg18UCSC Ensembl
Outerchr10:47093552..47102350hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg386799
hg196799
hg186799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688102
SamplesNA19239
Known GenesANTXRLP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3329341
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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