A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181301



Internal ID20748341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63000111..63031952hg38UCSC Ensembl
chr16:63034015..63065856hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3831842
hg1931842
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181301
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer