A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3350669



Internal ID14850933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46263010..46271408hg38UCSC Ensembl
Innerchr10:46264010..46270408hg38UCSC Ensembl
Outerchr10:46262010..46272408hg38UCSC Ensembl
chr10:47634246..47642644hg19UCSC Ensembl
Innerchr10:47635246..47641644hg19UCSC Ensembl
Outerchr10:47633246..47643644hg19UCSC Ensembl
chr10:47104252..47112650hg18UCSC Ensembl
Innerchr10:47105252..47111650hg18UCSC Ensembl
Outerchr10:47103252..47113650hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg388399
hg198399
hg188399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688104
SamplesNA19239
Known GenesANTXRLP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3350669
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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