A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109587



Internal ID22018820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:524551..524551hg38UCSC Ensembl
chr20:505195..505195hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626053
Samples
Known GenesCSNK2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109587
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