A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663793



Internal ID21612098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74910712..74910712hg38UCSC Ensembl
chr15:75203053..75203053hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097875
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663793
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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