A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602380



Internal ID21551038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89844221..89844272hg38UCSC Ensembl
chr15:90387453..90387504hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096016
SamplesHG03371
Known GenesAP3S2, C15orf38-AP3S2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602380
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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