A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088054



Internal ID21491350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58193849..58193849hg38UCSC Ensembl
chr15:58486048..58486048hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646284
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088054
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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