A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561904



Internal ID334871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72902608..72906549hg38UCSC Ensembl
chr5:72198435..72202376hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg383942
hg193942
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16967532
Samples
Known GenesTNPO1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561904
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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