A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554368



Internal ID327558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96602559..96602610hg38UCSC Ensembl
chr9:99364841..99364892hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386017
hg196017
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026814
Samples
Known GenesCDC14B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554368
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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