A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108568



Internal ID21284397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:27718558..27724705hg38UCSC Ensembl
Innerchr3:27760049..27766196hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg386148
hg196148
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116811
Supporting Variants
Samplessample360
Known GenesEOMES
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108568
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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