A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642027



Internal ID21590332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69367816..69367816hg38UCSC Ensembl
chr9:71982732..71982732hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162435
SamplesHG00513
Known GenesFAM189A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642027
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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