A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275021



Internal ID20484239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80054582..80054582hg38UCSC Ensembl
chr6:80764299..80764299hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764902
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275021
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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