A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226737



Internal ID20793777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130239322..130248621hg38UCSC Ensembl
chr9:133001601..133010900hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg389300
hg199300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226737
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