A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103799



Internal ID21479689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11425164..11425164hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3882
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663797
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103799
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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