A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760063



Internal ID20535923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86278743..86278743hg38UCSC Ensembl
chr16:86312349..86312349hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269702
Samples
Known GenesLINC01081
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760063
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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