A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659687



Internal ID21607992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25898786..25898786hg38UCSC Ensembl
chr15:26143933..26143933hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084529
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659687
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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