A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617151



Internal ID21809198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:137790..137852hg38UCSC Ensembl
chr16:187789..187851hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031533
Supporting Variants
Samples
Known GenesNPRL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617151
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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