A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087679



Internal ID21478409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25159142..25159142hg38UCSC Ensembl
chr15:25404289..25404289hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650514
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087679
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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