A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762658



Internal ID20538518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69379030..69379030hg38UCSC Ensembl
chr9:71993946..71993946hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278287
Samples
Known GenesFAM189A2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762658
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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