A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113848



Internal ID21297114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80848225..80880425hg38UCSC Ensembl
Innerchr10:82607981..82640181hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3832201
hg1932201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088492
Samplessample170
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113848
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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