A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538360



Internal ID21862715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170972587..170972587hg38UCSC Ensembl
chr3:170690376..170690376hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6069295
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538360
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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