A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069554



Internal ID21978787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6587440..6587440hg38UCSC Ensembl
chr4:6589167..6589167hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544935
Samples
Known GenesMAN2B2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069554
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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