A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090838



Internal ID21483878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43535113..43535175hg38UCSC Ensembl
chr15:43827311..43827373hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594513
Supporting Variants
SamplesNA12329
Known GenesPPIP5K1, RNU6-28P
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090838
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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