A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958024



Internal ID22733110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101238293..101238293hg38UCSC Ensembl
chr9:104000575..104000575hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446939
Samples
Known GenesLPPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958024
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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