A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683054



Internal ID21204911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52248857..52248857hg38UCSC Ensembl
chr16:52282769..52282769hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2796029
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683054
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.633333


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