A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659350



Internal ID21607655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33817878..33817878hg38UCSC Ensembl
chr11:33839424..33839424hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074570
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659350
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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