A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278063



Internal ID20487281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80042582..80042582hg38UCSC Ensembl
chr6:80752299..80752299hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760343
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278063
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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