A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135534



Internal ID21486698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24813599..24813599hg38UCSC Ensembl
chr3:24855090..24855090hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621605
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135534
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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