A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452338



Internal ID230494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177934482..177936770hg38UCSC Ensembl
chr3:177652270..177654558hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg382289
hg192289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943629
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452338
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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