A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182942



Internal ID20749982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19890520..19907282hg38UCSC Ensembl
chr16:19901842..19918604hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3816763
hg1916763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496646
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182942
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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