A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546905



Internal ID21871260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89755851..89758129hg38UCSC Ensembl
chr4:90677002..90679280hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg382279
hg192279
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998456
Supporting Variants
Samples
Known GenesSNCA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546905
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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