A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068926



Internal ID21978159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:49926438..49926438hg38UCSC Ensembl
chr8:50838998..50838998hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg382501
hg192501
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586306
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068926
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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