A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951676



Internal ID35144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89756022..89758358hg38UCSC Ensembl
chr4:90677173..90679509hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg382337
hg192337
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140374
Supporting Variants
Samples
Known GenesSNCA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951676
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001562


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