A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602867



Internal ID21794914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108258223..108258223hg38UCSC Ensembl
chr13:108910571..108910571hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093916
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602867
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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