A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192685



Internal ID20759725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25081261..25097302hg38UCSC Ensembl
chr13:25655399..25671440hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3816042
hg1916042
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480859
Supporting Variants
Samples
Known GenesPABPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192685
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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