A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765223



Internal ID20541083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169079778..169079778hg38UCSC Ensembl
chr5:168506783..168506783hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269655
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765223
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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