A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451289



Internal ID229475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145090934..145177291hg38UCSC Ensembl
chr3:144808708..144895078hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3886358
hg1986371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940710
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451289
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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