A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662289



Internal ID21610594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65011000..65011000hg38UCSC Ensembl
chr16:65044903..65044903hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090972
SamplesHG03065
Known GenesCDH11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662289
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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