A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181915



Internal ID20748955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131917001..131936400hg38UCSC Ensembl
chr12:132401546..132420945hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3819400
hg1919400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489387
Supporting Variants
Samples
Known GenesPUS1, ULK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181915
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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