A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652470



Internal ID21600775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45577321..45577321hg38UCSC Ensembl
chr15:45869519..45869519hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081726
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652470
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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