A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469802



Internal ID247579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11165965..11176911hg38UCSC Ensembl
chr5:11166077..11177023hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3810947
hg1910947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961780
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469802
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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