A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162298



Internal ID21489483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5471950..5471950hg38UCSC Ensembl
chr9:5471950..5471950hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381434
hg191434
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637819
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162298
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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