A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644998



Internal ID21837045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5251245..5255758hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051347
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644998
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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