A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453712



Internal ID231826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139027574..139067574hg38UCSC Ensembl
chr3:138746416..138786416hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3840001
hg1940001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940982
Samples
Known GenesPRR23C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453712
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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