A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5400484



Internal ID179865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77420384..77420435hg38UCSC Ensembl
chr5:76716209..76716260hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968459
Samples
Known GenesPDE8B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5400484
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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