A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080289



Internal ID21989522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30786497..30786497hg38UCSC Ensembl
chr8:30644013..30644013hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559752
Samples
Known GenesPPP2CB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080289
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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