A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583816



Internal ID21775859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60518561..60527334hg38UCSC Ensembl
chr9_gl000199_random:3..8776hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388774
hg198774
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003363
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583816
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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