A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010239



Internal ID21919582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65429328..65436303hg38UCSC Ensembl
chr8:66341563..66348538hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg386976
hg196976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593856
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010239
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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