A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488590



Internal ID265895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4199436..4199505hg38UCSC Ensembl
chr9:4199436..4199505hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17017849
Samples
Known GenesGLIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488590
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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