A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597923



Internal ID21789967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23453401..23454880hg38UCSC Ensembl
chr16:23464722..23466201hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381480
hg191480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033807
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597923
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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