A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761986



Internal ID20537846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53300964..53300964hg38UCSC Ensembl
chr18:50827334..50827334hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274627
Samples
Known GenesDCC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761986
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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