A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479049



Internal ID22536951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67053265..67054800hg38UCSC Ensembl
chr16:67087168..67088703hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381536
hg191536
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870619
Supporting Variants
Samples
Known GenesCBFB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479049
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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