A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796395



Internal ID21241733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86034225..86034225hg38UCSC Ensembl
chr16:86067831..86067831hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13684875
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796395
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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