A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755459



Internal ID20531319
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 StatusM
Merged Variants
Supporting Variantsnssv16290332
Samples
Known GenesFAM189A2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755459
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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