A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409825



Internal ID189145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74301035..74301055hg38UCSC Ensembl
chr5:73596860..73596880hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16966887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409825
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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