A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627982



Internal ID21576287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33511234..33511234hg38UCSC Ensembl
chr9:33511232..33511232hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg389202
hg199202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162162
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627982
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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