A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062697



Internal ID21971930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152726306..152726306hg38UCSC Ensembl
chr5:152105866..152105866hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg382588
hg192588
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062697
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer