A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459719



Internal ID237729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181256030..181257790hg38UCSC Ensembl
chr5:180683031..180684791hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg381761
hg191761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977897
Samples
Known GenesTRIM52
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459719
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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