A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542021



Internal ID21866376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10976153..10976208hg38UCSC Ensembl
chr5:10976265..10976320hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998765
Supporting Variants
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542021
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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