A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179173



Internal ID20746213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:732016..759219hg38UCSC Ensembl
chr16:782016..809219hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3827204
hg1927204
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508589
Supporting Variants
Samples
Known GenesNARFL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179173
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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