A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610294



Internal ID21802341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:138505..138505hg38UCSC Ensembl
chr16:188504..188504hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086841
Supporting Variants
Samples
Known GenesNPRL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610294
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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