A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281173



Internal ID20490391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157179118..157179118hg38UCSC Ensembl
chr3:156896907..156896907hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765842
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281173
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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