A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3360056



Internal ID15207035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:81106353..81106387hg38UCSC Ensembl
Innerchr10:81106357..81106381hg38UCSC Ensembl
Outerchr10:81106325..81106415hg38UCSC Ensembl
chr10:82866109..82866143hg19UCSC Ensembl
Innerchr10:82866113..82866137hg19UCSC Ensembl
Outerchr10:82866081..82866171hg19UCSC Ensembl
chr10:82856089..82856123hg18UCSC Ensembl
Innerchr10:82856117..82856093hg18UCSC Ensembl
Outerchr10:82856061..82856151hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38282
hg19282
hg18282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8949574, essv8949575, essv8949576, essv8949578, essv8949577
SamplesNA18856, NA18912, NA18517, NA19093, NA18511
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3360056
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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