A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17017856



Internal ID79556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4273317..4420917hg38UCSC Ensembl
chr9:4273317..4420917hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38147601
hg19147601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492360
Supporting Variants
Samples
Known GenesGLIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17017856
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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