A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179411



Internal ID20746451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3982008..3982631hg38UCSC Ensembl
chr9:3982008..3982631hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426099
Supporting Variants
Samples
Known GenesGLIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179411
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00126


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