A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220579



Internal ID20787619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113305034..113307091hg38UCSC Ensembl
chr9:116067314..116069371hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382058
hg192058
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449946
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220579
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