A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267134



Internal ID20476352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167684965..167684965hg38UCSC Ensembl
chr3:167402753..167402753hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758912
Supporting Variants
Samples
Known GenesPDCD10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267134
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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