A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263784



Internal ID20473002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107391206..107391206hg38UCSC Ensembl
chr3:107110053..107110053hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263784
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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