A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026219



Internal ID85216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110962849..110962900hg38UCSC Ensembl
chr9:113725129..113725180hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg386017
hg196017
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561816
Supporting Variants
Samples
Known GenesLPAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026219
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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