A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592146



Internal ID21784189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69367649..69367649hg38UCSC Ensembl
chr9:71982565..71982565hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089021
Supporting Variants
Samples
Known GenesFAM189A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592146
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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