A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162435



Internal ID21412453
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 StatusS
Merged Variantsnsv5642027
Supporting Variants
SamplesHG00513
Known GenesFAM189A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162435
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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