A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182876



Internal ID20749916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11642767..11696423hg38UCSC Ensembl
chr16:11736623..11790279hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3853657
hg1953657
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512634
Supporting Variants
Samples
Known GenesSNN, TXNDC11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182876
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