A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095930



Internal ID21283149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68054738..68081897hg38UCSC Ensembl
Innerchr13:68628870..68656029hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3827160
hg1927160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113621
Supporting Variants
Samplessample339
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095930
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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