A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586029



Internal ID21534578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63319320..63319373hg38UCSC Ensembl
chr11:63086792..63086845hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075607
SamplesHG00732
Known GenesMIR3680-1, MIR3680-2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586029
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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