A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182292



Internal ID20749332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47144401..47151100hg38UCSC Ensembl
chr16:47178312..47185011hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503915
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182292
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00061


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