A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391856



Internal ID21049409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89753688..89767608hg38UCSC Ensembl
chr4:90674839..90688759hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3813921
hg1913921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215228
Samples
Known GenesSNCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391856
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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