A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560119



Internal ID21884474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161557223..161564383hg38UCSC Ensembl
chr5:160984229..160991389hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg387161
hg197161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019707
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560119
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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