A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463359



Internal ID241265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66904253..66906462hg38UCSC Ensembl
chr5:66200081..66202290hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg382210
hg192210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16966144
Samples
Known GenesMAST4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463359
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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