A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3332605



Internal ID14832878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46300610..46304308hg38UCSC Ensembl
Innerchr10:46301610..46303308hg38UCSC Ensembl
Outerchr10:46299610..46305308hg38UCSC Ensembl
chr10:47671846..47675544hg19UCSC Ensembl
Innerchr10:47672846..47674544hg19UCSC Ensembl
Outerchr10:47670846..47676544hg19UCSC Ensembl
chr10:47141852..47145550hg18UCSC Ensembl
Innerchr10:47142852..47144550hg18UCSC Ensembl
Outerchr10:47140852..47146550hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg383699
hg193699
hg183699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688107
SamplesNA19239
Known GenesANTXRL
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3332605
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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