A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079145



Internal ID21988378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110721673..110721673hg38UCSC Ensembl
chr5:110057374..110057374hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553726
Samples
Known GenesTMEM232
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079145
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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