A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463919



Internal ID241809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168034543..168035332hg38UCSC Ensembl
chr5:167461548..167462337hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977105
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463919
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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