A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951674



Internal ID35142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89736342..89738562hg38UCSC Ensembl
chr4:90657493..90659713hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg382221
hg192221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463765
Supporting Variants
Samples
Known GenesSNCA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951674
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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