A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3374054



Internal ID14874316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46261010..46262508hg38UCSC Ensembl
Innerchr10:46261508..46262010hg38UCSC Ensembl
Outerchr10:46260010..46263508hg38UCSC Ensembl
chr10:47632246..47633744hg19UCSC Ensembl
Innerchr10:47632744..47633246hg19UCSC Ensembl
Outerchr10:47631246..47634744hg19UCSC Ensembl
chr10:47102252..47103750hg18UCSC Ensembl
Innerchr10:47103252..47102750hg18UCSC Ensembl
Outerchr10:47101252..47104750hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688103
SamplesNA19239
Known GenesANTXRLP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3374054
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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