A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617454



Internal ID21809501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43082995..43082995hg38UCSC Ensembl
chr13:43657131..43657131hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg385911
hg195911
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081509
Supporting Variants
Samples
Known GenesDNAJC15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617454
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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