A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096153



Internal ID21450681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24848258..24848258hg38UCSC Ensembl
chr15:25093405..25093405hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662981
Supporting Variants
SamplesHG01505
Known GenesSNRPN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096153
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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