A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668291



Internal ID21616596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37509602..37509602hg38UCSC Ensembl
chr22:37905609..37905609hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135699
SamplesHG03732
Known GenesCARD10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668291
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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