A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484763



Internal ID262170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110896996..110926059hg38UCSC Ensembl
chr9:113659276..113688339hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3829064
hg1929064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026211
Samples
Known GenesLPAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484763
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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