A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296464



Internal ID20505682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47860013..47860013hg38UCSC Ensembl
chr16:47893924..47893924hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763187
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296464
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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