A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8677716



Internal ID15100770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:81106364..81106383hg38UCSC Ensembl
Innerchr10:81106360..81106387hg38UCSC Ensembl
Outerchr10:81106341..81106406hg38UCSC Ensembl
chr10:82866120..82866139hg19UCSC Ensembl
Innerchr10:82866116..82866143hg19UCSC Ensembl
Outerchr10:82866097..82866162hg19UCSC Ensembl
chr10:82856100..82856119hg18UCSC Ensembl
Innerchr10:82856123..82856096hg18UCSC Ensembl
Outerchr10:82856077..82856142hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3378852
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8677716
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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