A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652855



Internal ID21601160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42034346..42034346hg38UCSC Ensembl
chr11:42055896..42055896hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074987
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652855
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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