A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096152



Internal ID22005385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78879309..78879309hg38UCSC Ensembl
chr11:78590354..78590354hg19UCSC 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 Variantsnssv17588825
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096152
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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