A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664698



Internal ID21613004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35389339..35389339hg38UCSC Ensembl
chr22:35785332..35785332hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129683
SamplesHG03065
Known GenesHMOX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664698
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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