A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026814



Internal ID85596
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 StatusS
Merged Variantsnsv5554368
Supporting Variants
Samples
Known GenesCDC14B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026814
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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