A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589692



Internal ID21538258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42131788..42141616hg38UCSC Ensembl
chr15:42423986..42433814hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg389829
hg199829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086539
SamplesNA18939
Known GenesPLA2G4F
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589692
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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