A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260852



Internal ID20470070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91709289..91709289hg38UCSC Ensembl
chr5:91005106..91005106hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg385913
hg195913
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750540
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260852
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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