A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080266



Internal ID21989499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14689431..14689431hg38UCSC Ensembl
chr5:14689540..14689540hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555761
Samples
Known GenesFAM105B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080266
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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