A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761555



Internal ID20537415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:115162010..115162010hg38UCSC Ensembl
chr9:117924289..117924289hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276072
Samples
Known GenesDEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761555
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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