A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269260



Internal ID20478478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11128161..11135129hg38UCSC Ensembl
chr5:11128273..11135241hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg386969
hg196969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749308
Supporting Variants
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269260
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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