A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194856



Internal ID20761896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3555125..3560352hg38UCSC Ensembl
chr16:3605126..3610353hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385228
hg195228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513511
Supporting Variants
Samples
Known GenesNLRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194856
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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