A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468225



Internal ID246026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153323868..153323989hg38UCSC Ensembl
chr5:152703428..152703549hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16975704
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468225
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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