A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5403926



Internal ID183285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9542528..9542579hg38UCSC Ensembl
chr11:9564075..9564126hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688342
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5403926
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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