A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078769



Internal ID21988002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42299116..42299116hg38UCSC Ensembl
chr6:42266854..42266854hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563217
Samples
Known GenesTRERF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078769
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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