A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624908



Internal ID21816955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46735139..46735139hg38UCSC Ensembl
chr19:47238396..47238396hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108185
Supporting Variants
Samples
Known GenesSTRN4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624908
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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