A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042464



Internal ID21951780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41864584..41866790hg38UCSC Ensembl
chr21:43284693..43286899hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382207
hg192207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647657
Samples
Known GenesPRDM15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042464
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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