A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231745



Internal ID20798785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37889901..37893800hg38UCSC Ensembl
chr9:37889898..37893797hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447437
Supporting Variants
Samples
Known GenesSLC25A51
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231745
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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