A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998767



Internal ID21908110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11310791..11310912hg38UCSC Ensembl
chr5:11310903..11311024hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538260
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998767
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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