A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064471



Internal ID21973704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53083421..53083421hg38UCSC Ensembl
chr6:52948219..52948219hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg381551
hg191551
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567208
Samples
Known GenesFBXO9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064471
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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