A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419139



Internal ID198285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145285000..145290587hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419139
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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