A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766557



Internal ID20542417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172978581..172978581hg38UCSC Ensembl
chr5:172405584..172405584hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766557
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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