A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965927



Internal ID22740862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99862549..99862549hg38UCSC Ensembl
chr9:102624831..102624831hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440763
Samples
Known GenesNR4A3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965927
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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