A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027390



Internal ID21936733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57475666..57475737hg38UCSC Ensembl
chr16:57509578..57509649hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635308
Samples
Known GenesDOK4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027390
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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