A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031388



Internal ID21940731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14890600..14890732hg38UCSC Ensembl
chr11:14912146..14912278hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588504
Samples
Known GenesCYP2R1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031388
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