A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663807



Internal ID21612112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74991160..74991160hg38UCSC Ensembl
chr15:75283501..75283501hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082638
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663807
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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