A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262168



Internal ID20471386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13682058..13682058hg38UCSC Ensembl
chr3:13723557..13723557hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761704
Supporting Variants
Samples
Known GenesLINC00620
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262168
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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