A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3335392



Internal ID14835665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79159617..79159636hg38UCSC Ensembl
Innerchr10:79159613..79159640hg38UCSC Ensembl
Outerchr10:79159594..79159659hg38UCSC Ensembl
chr10:80919374..80919393hg19UCSC Ensembl
Innerchr10:80919370..80919397hg19UCSC Ensembl
Outerchr10:80919351..80919416hg19UCSC Ensembl
chr10:80589380..80589399hg18UCSC Ensembl
Innerchr10:80589403..80589376hg18UCSC Ensembl
Outerchr10:80589357..80589422hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg386000
hg196000
hg186000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9648569
SamplesNA18970
Known GenesZMIZ1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3335392
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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