A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761278



Internal ID20537138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167030242..167030242hg38UCSC Ensembl
chr1:166999479..166999479hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761278
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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