A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458228



Internal ID236257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138895607..138897449hg38UCSC Ensembl
chr5:138231296..138233138hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg381843
hg191843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974097
Samples
Known GenesCTNNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458228
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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