A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001199



Internal ID21910542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110892679..110892807hg38UCSC Ensembl
chr9:113654959..113655087hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596669
Samples
Known GenesLPAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001199
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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