A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264371



Internal ID20473589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107887391..107887391hg38UCSC Ensembl
chr13:108539739..108539739hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758719
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264371
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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