A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537686



Internal ID21862041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11348663..11348663hg38UCSC Ensembl
chr5:11348775..11348775hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073187
Supporting Variants
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537686
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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