A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275381



Internal ID20484599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116346810..116346810hg38UCSC Ensembl
chr11:116217527..116217527hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750318
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275381
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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