A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5408976



Internal ID188299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108000386..108000437hg38UCSC Ensembl
chr9:110762667..110762718hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5408976
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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