A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547978



Internal ID21872333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133375291..133375291hg38UCSC Ensembl
chr5:132710983..132710983hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067579
Supporting Variants
Samples
Known GenesFSTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547978
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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