A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484924



Internal ID262323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131115734..131116032hg38UCSC Ensembl
chr9:133991121..133991419hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028931
Samples
Known GenesAIF1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484924
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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