A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059300



Internal ID21968534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23851656..23851656hg38UCSC Ensembl
chr1:24178146..24178146hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527415
Samples
Known GenesFUCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059300
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