A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195618



Internal ID20762658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57298484..57304930hg38UCSC Ensembl
chr16:57332396..57338842hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg386447
hg196447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195618
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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