A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660417



Internal ID21608722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88897514..88897514hg38UCSC Ensembl
chr15:89440745..89440745hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084364, nssv17093533
SamplesHG00731, HG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660417
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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