A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450005



Internal ID228224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190361924..190369891hg38UCSC Ensembl
chr3:190079713..190087680hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg387968
hg197968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944415
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450005
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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