A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487808



Internal ID265138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66167616..66167698hg38UCSC Ensembl
chr10:67927374..67927456hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035587
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487808
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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