A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177844



Internal ID20744884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13852437..13911913hg38UCSC Ensembl
chr16:13946294..14005770hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3859477
hg1959477
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511694
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177844
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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