A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264494



Internal ID20473712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11348661..11348661hg38UCSC Ensembl
chr5:11348773..11348773hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752351
Supporting Variants
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264494
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