A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612954



Internal ID21805001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101161539..101422432hg38UCSC Ensembl
chr13:101813890..102074783hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38260894
hg19260894
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026959
Supporting Variants
Samples
Known GenesNALCN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612954
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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