A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646866



Internal ID21595171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92829521..92829521hg38UCSC Ensembl
chr15:93372751..93372751hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092024
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646866
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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