A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218319



Internal ID20785359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3663092..3866427hg38UCSC Ensembl
chr9:3663092..3866427hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38203336
hg19203336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419549
Supporting Variants
Samples
Known GenesGLIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218319
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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