A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080058



Internal ID21989291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118798372..118798372hg38UCSC Ensembl
chr4:119719527..119719527hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg383196
hg193196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549703
Samples
Known GenesSEC24D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080058
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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