A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841314



Internal ID22024957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110959185..110959185hg38UCSC Ensembl
chr9:113721465..113721465hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240138
Supporting Variants
Samples
Known GenesLPAR1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841314
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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