A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5394889



Internal ID174315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94704584..94704635hg38UCSC Ensembl
chr5:94040289..94040340hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16972340
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5394889
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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