A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617309



Internal ID21809356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18867873..18867943hg38UCSC Ensembl
chr16:18879195..18879265hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031991
Supporting Variants
Samples
Known GenesSMG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617309
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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