A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061809



Internal ID21971042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149705344..149705344hg38UCSC Ensembl
chr5:149084907..149084907hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061809
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