A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296116



Internal ID20505334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148439565..148439565hg38UCSC Ensembl
chr5:147819128..147819128hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751353
Supporting Variants
Samples
Known GenesFBXO38
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296116
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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