A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281956



Internal ID20491174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138616241..138616241hg38UCSC Ensembl
chr3:138335083..138335083hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757704
Supporting Variants
Samples
Known GenesFAIM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281956
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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