A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137980



Internal ID21464129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27092905..27093725hg38UCSC Ensembl
chr3:27134396..27135216hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574879
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137980
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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