A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586328



Internal ID21534880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41383301..41383478hg38UCSC Ensembl
chr15:41675499..41675676hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086580
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586328
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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