A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459593



Internal ID237606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150109324..150111184hg38UCSC Ensembl
chr5:149488887..149490747hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381861
hg191861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974758
Samples
Known GenesCSF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459593
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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