A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5403435



Internal ID182795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165233533..165233584hg38UCSC Ensembl
chr5:164660539..164660590hg19UCSC Ensembl
Cytoband5q34
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 Variantsnssv16976599
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5403435
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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