A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621586



Internal ID21813633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53383991..53427419hg38UCSC Ensembl
chr16:53417903..53461331hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3843429
hg1943429
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621586
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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