A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638478



Internal ID21586783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91510812..91510812hg38UCSC Ensembl
chr9:94273094..94273094hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163394
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638478
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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