A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290332



Internal ID20499550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69367742..69367742hg38UCSC Ensembl
chr9:71982658..71982658hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755459
Supporting Variants
Samples
Known GenesFAM189A2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290332
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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