A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652360



Internal ID21600665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68750943..68750943hg38UCSC Ensembl
chr11:68518411..68518411hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075507
SamplesHG02011
Known GenesMTL5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652360
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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