A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274619



Internal ID20483837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36879557..36879557hg38UCSC Ensembl
chr3:36921048..36921048hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754437
Supporting Variants
Samples
Known GenesTRANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274619
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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