A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221970



Internal ID20789010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16368732..16377069hg38UCSC Ensembl
chr9:16368730..16377067hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg388338
hg198338
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425807
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221970
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