A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195909



Internal ID20762949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108539333..108542325hg38UCSC Ensembl
chr12:108933109..108936101hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg382993
hg192993
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493811
Supporting Variants
Samples
Known GenesSART3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195909
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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