A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603805



Internal ID21795852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97571564..97571564hg38UCSC Ensembl
chr13:98223818..98223818hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093300
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603805
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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