A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027129



Internal ID21936472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67045889..67045951hg38UCSC Ensembl
chr16:67079792..67079854hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630607
Samples
Known GenesCBFB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027129
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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