A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264091



Internal ID20473309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104756234..104756234hg38UCSC Ensembl
chr13:105408585..105408585hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4768235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264091
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer