A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088225



Internal ID21997458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78853066..78853066hg38UCSC Ensembl
chr11:78564111..78564111hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587370
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088225
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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