A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073187



Internal ID21982420
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 StatusM
Merged Variants
Supporting Variantsnssv17537686
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073187
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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