A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489362



Internal ID266645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107709700..107714017hg38UCSC Ensembl
chr9:110471981..110476298hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg384318
hg194318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489362
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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