A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474259



Internal ID251921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97605839..97618918hg38UCSC Ensembl
chr9:100368121..100381200hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3813080
hg1913080
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027573
Samples
Known GenesTSTD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474259
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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