A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191818



Internal ID20758858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83518315..83941761hg38UCSC Ensembl
chr16:83551920..83975366hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38423447
hg19423447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503433
Supporting Variants
Samples
Known GenesCDH13, HSBP1, MLYCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191818
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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