A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594212



Internal ID21542808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1486837..1486938hg38UCSC Ensembl
chr11:1508067..1508168hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073215
SamplesHG02587
Known GenesMOB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594212
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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