A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913316



Internal ID22688532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61358555..61360806hg38UCSC Ensembl
chr11:61126027..61128278hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg382252
hg192252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361322
Samples
Known GenesCYB561A3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913316
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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