A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409521



Internal ID188842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83778744..83778795hg38UCSC Ensembl
chr9:86393659..86393710hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025414
Samples
Known GenesGKAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409521
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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