A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585814



Internal ID21534362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36144853..36145106hg38UCSC Ensembl
chr11:36166403..36166656hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074379
SamplesHG00731
Known GenesLDLRAD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585814
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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