A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178329



Internal ID20745369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3351095..3427692hg38UCSC Ensembl
chr16:3401095..3477692hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3876598
hg1976598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509003
Supporting Variants
Samples
Known GenesMTRNR2L4, OR2C1, ZNF174, ZSCAN32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178329
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