A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185731



Internal ID20752771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67370558..67373958hg38UCSC Ensembl
chr16:67404461..67407861hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383401
hg193401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505700
Supporting Variants
Samples
Known GenesLRRC36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185731
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