A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280168



Internal ID20489386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121961698..121961698hg38UCSC Ensembl
chr5:121297393..121297393hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280168
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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