A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088733



Internal ID21997966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69379025..69379025hg38UCSC Ensembl
chr9:71993941..71993941hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587828
Samples
Known GenesFAM189A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088733
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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