A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037969



Internal ID21947312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28080547..28100211hg38UCSC Ensembl
chr13:28654684..28674348hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3819665
hg1919665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610859
Samples
Known GenesFLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037969
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