A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218481



Internal ID20785521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19306585..19403955hg38UCSC Ensembl
chr9:19306583..19403953hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3897371
hg1997371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428985
Supporting Variants
Samples
Known GenesDENND4C, RPS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218481
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