A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082787



Internal ID21992020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103760096..103760096hg38UCSC Ensembl
chr14:104226433..104226433hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599707
Samples
Known GenesPPP1R13B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082787
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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