A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5538663



Internal ID313722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96581501..96581538hg38UCSC Ensembl
chr9:99343783..99343820hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026810
Samples
Known GenesCDC14B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5538663
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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