A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132385



Internal ID21466597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42192400..42192400hg38UCSC Ensembl
chr3:42233892..42233892hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621350
Supporting Variants
SamplesHG03065
Known GenesTRAK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132385
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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