A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181841



Internal ID20748881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47005250..47006120hg38UCSC Ensembl
chr16:47039161..47040031hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501132
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181841
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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