A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430793



Internal ID209587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62834950..62896832hg38UCSC Ensembl
chr9:66490774..66552656hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3861883
hg1961883
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023071
Samples
Known GenesPTGER4P2-CDK2AP2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430793
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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