A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379923



Internal ID21037476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108627056..108652858hg38UCSC Ensembl
chr4:109548212..109574014hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3825803
hg1925803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209508
Samples
Known GenesOSTC, RPL34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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