A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132437



Internal ID21466642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14249659..14254563hg38UCSC Ensembl
chr3:14291159..14296063hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg384905
hg194905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580258
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132437
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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