A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895781



Internal ID22670868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89756058..89758339hg38UCSC Ensembl
chr4:90677209..90679490hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg382282
hg192282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416956
Samples
Known GenesSNCA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895781
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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