A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487972



Internal ID265294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67502885..67584342hg38UCSC Ensembl
chr10:69262643..69344100hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3881458
hg1981458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037327
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487972
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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