A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016556



Internal ID21925899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150173448..150175495hg38UCSC Ensembl
chr5:149553011..149555058hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573808
Samples
Known GenesCDX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016556
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