A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591825



Internal ID21540403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45111212..45111404hg38UCSC Ensembl
chr11:45132763..45132955hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074707
SamplesHG00731
Known GenesPRDM11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591825
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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