A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026211



Internal ID85211
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 StatusS
Merged Variantsnsv5484763
Supporting Variants
Samples
Known GenesLPAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026211
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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