A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074379



Internal ID21438105
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 StatusS
Merged Variantsnsv5585814
Supporting Variants
SamplesHG00731
Known GenesLDLRAD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074379
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