A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176862



Internal ID20743902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128198826..128201346hg38UCSC Ensembl
chr9:130961105..130963625hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382521
hg192521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439235
Supporting Variants
Samples
Known GenesCIZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00362


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer