A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660284



Internal ID21608589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28225951..28225951hg38UCSC Ensembl
chr15:28471097..28471097hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097062
SamplesHG00513
Known GenesHERC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660284
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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