A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597855



Internal ID21546475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69300581..69300840hg38UCSC Ensembl
chr15:69592920..69593179hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084015
SamplesNA18939
Known GenesPAQR5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597855
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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