A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084639



Internal ID21435244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98437681..98437681hg38UCSC Ensembl
chr15:98980910..98980910hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663856
Supporting Variants
SamplesHG00731
Known GenesFAM169B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084639
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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