A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489383



Internal ID266666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83804890..83804959hg38UCSC Ensembl
chr9:86419805..86419874hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025418
Samples
Known GenesGKAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489383
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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