A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661583



Internal ID21609888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89479122..89479122hg38UCSC Ensembl
chr15:90022353..90022353hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083008
SamplesHG03486
Known GenesRHCG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661583
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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