A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754312



Internal ID20530172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118678537..118678537hg38UCSC Ensembl
chr11:118549246..118549246hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263871
Samples
Known GenesTREH
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754312
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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