A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409722



Internal ID189042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100970372..100970372hg38UCSC Ensembl
chr4:101891529..101891529hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16953345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409722
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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