A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5407411



Internal ID186745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79119024..79119075hg38UCSC Ensembl
chr11:78830069..78830120hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048669
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5407411
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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