A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593132



Internal ID21541717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14879524..14879639hg38UCSC Ensembl
chr11:14901070..14901185hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073216
SamplesHG03125
Known GenesCYP2R1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593132
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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