A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137630



Internal ID21481859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133384323..133384323hg38UCSC Ensembl
chr3:133103167..133103167hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624243
Supporting Variants
SamplesHG03683
Known GenesTMEM108
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137630
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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