A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439716



Internal ID218248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141062836..141062992hg38UCSC Ensembl
chr3:140781678..140781834hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940337
Samples
Known GenesSPSB4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439716
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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