A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5548834



Internal ID322551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117843403..117843403hg38UCSC Ensembl
chr9:120605681..120605681hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027879
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5548834
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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