A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191426



Internal ID20758466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68488302..68495544hg38UCSC Ensembl
chr16:68522205..68529447hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg387243
hg197243
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191426
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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