A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183790



Internal ID20750830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47540858..47563209hg38UCSC Ensembl
chr16:47574769..47597120hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3822352
hg1922352
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506912
Supporting Variants
Samples
Known GenesPHKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183790
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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