A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5394761



Internal ID174188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105429845..105429845hg38UCSC Ensembl
chr9:108192126..108192126hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025090
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5394761
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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