A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069712



Internal ID21978945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173891179..173891179hg38UCSC Ensembl
chr5:173318182..173318182hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567886
Samples
Known GenesCPEB4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069712
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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