A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587080



Internal ID21535639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97989391..97993238hg38UCSC Ensembl
chr15:98532621..98536468hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg383848
hg193848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086849
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587080
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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