A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3414928



Internal ID14915201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84765478..84765489hg38UCSC Ensembl
Innerchr16:84765480..84765487hg38UCSC Ensembl
Outerchr16:84765476..84765491hg38UCSC Ensembl
chr16:84799084..84799095hg19UCSC Ensembl
Innerchr16:84799086..84799093hg19UCSC Ensembl
Outerchr16:84799082..84799097hg19UCSC Ensembl
chr16:83356585..83356596hg18UCSC Ensembl
Innerchr16:83356587..83356594hg18UCSC Ensembl
Outerchr16:83356583..83356598hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865940, essv7865939
SamplesNA18520, NA11992
Known GenesUSP10
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3414928
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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