A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3435780



Internal ID14936048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46305010..46330508hg38UCSC Ensembl
Innerchr10:46306010..46329508hg38UCSC Ensembl
Outerchr10:46304010..46331508hg38UCSC Ensembl
chr10:47676246..47701744hg19UCSC Ensembl
Innerchr10:47677246..47700744hg19UCSC Ensembl
Outerchr10:47675246..47702744hg19UCSC Ensembl
chr10:47146252..47171750hg18UCSC Ensembl
Innerchr10:47147252..47170750hg18UCSC Ensembl
Outerchr10:47145252..47172750hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3825499
hg1925499
hg1825499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688109
SamplesNA19239
Known GenesANTXRL
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3435780
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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