A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961794



Internal ID41831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11310867..11311381hg38UCSC Ensembl
chr5:11310979..11311493hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472533
Supporting Variants
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961794
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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