A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651678



Internal ID21599983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18053887..18053887hg38UCSC Ensembl
chr11:18075434..18075434hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073831
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651678
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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