A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5445012



Internal ID223373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141204966..141211400hg38UCSC Ensembl
chr3:140923808..140930242hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg386435
hg196435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940342
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5445012
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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