A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098342



Internal ID22007575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99855556..99855556hg38UCSC Ensembl
chr9:102617838..102617838hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581001
Samples
Known GenesNR4A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098342
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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