A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622618



Internal ID21814665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71519434..71530020hg38UCSC Ensembl
chr16:71553337..71563923hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3810587
hg1910587
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037179
Supporting Variants
Samples
Known GenesCHST4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622618
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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