A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099859



Internal ID22009092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6486648..6486648hg38UCSC Ensembl
chr9:6486648..6486648hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577733
Samples
Known GenesUHRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099859
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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