A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551517



Internal ID21875872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32826695..32826695hg38UCSC Ensembl
chr5:32826801..32826801hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6078304
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551517
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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