A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591790



Internal ID21783833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110968484..110969188hg38UCSC Ensembl
chr9:113730764..113731468hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016403
Supporting Variants
Samples
Known GenesLPAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591790
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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