A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485296



Internal ID262690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93150826..93154180hg38UCSC Ensembl
chr9:95913108..95916462hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg383355
hg193355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485296
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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