A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3367444



Internal ID15214420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84177016..84180014hg38UCSC Ensembl
Innerchr10:84178016..84179014hg38UCSC Ensembl
Outerchr10:84176016..84181014hg38UCSC Ensembl
chr10:85936772..85939770hg19UCSC Ensembl
Innerchr10:85937772..85938770hg19UCSC Ensembl
Outerchr10:85935772..85940770hg19UCSC Ensembl
chr10:85926752..85929750hg18UCSC Ensembl
Innerchr10:85927752..85928750hg18UCSC Ensembl
Outerchr10:85925752..85930750hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg382999
hg192999
hg182999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688145
SamplesNA19240
Known GenesC10orf99
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3367444
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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