A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666365



Internal ID21614670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29120722..29120722hg38UCSC Ensembl
chr22:29516710..29516710hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg382460
hg192460
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126585
SamplesHG01596
Known GenesKREMEN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666365
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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