A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084015



Internal ID21488820
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 StatusS
Merged Variantsnsv5597855
Supporting Variants
SamplesNA18939
Known GenesPAQR5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084015
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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