A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460534



Internal ID238513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164439887..164446688hg38UCSC Ensembl
chr5:163866893..163873694hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg386802
hg196802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16975350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460534
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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